This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA2460202840
Gene: SLC9A6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136039909C= , CM000685.2:g.136039909C= GRCh38
NC_000023.10:g.135122068C= , CM000685.1:g.135122068C= GRCh37
NC_000023.9:g.134949734C= NCBI36
NG_017160.1:g.59483C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370695.8:c.1728-167C= ENSP00000359729.4:n.1728-167C=
ENST00000370701.6:c.1572-167C= ENSP00000359735.1:n.1572-167C=
ENST00000630721.3:c.1662-167C= MANE Select ENSP00000487486.2:n.1662-167C=
ENST00000636092.1:c.1572-167C= ENSP00000490406.1:n.1572-167C=
ENST00000636206.2:n.902-167C=
ENST00000636347.1:c.1572-167C= ENSP00000490648.1:n.1572-167C=
ENST00000636625.1:n.563-167C=
ENST00000636798.1:n.1007-167C=
ENST00000637195.1:c.1476-167C= ENSP00000490330.1:n.1476-167C=
ENST00000637234.1:c.1572-167C= ENSP00000490527.1:n.1572-167C=
ENST00000637581.1:c.1572-167C= ENSP00000490731.1:n.1572-167C=
ENST00000638078.1:c.60-135C=
ENST00000676233.1:n.728C=
ENST00000678163.1:c.1818-167C= ENSP00000502845.1:n.1818-167C=
ENST00000370695.6:c.1728-167C= ENSP00000359729.4:n.1728-167C=
ENST00000370698.7:c.1632-167C= ENSP00000359732.3:n.1632-167C=
ENST00000370701.5:c.1572-167C= ENSP00000359735.1:n.1572-167C=
ENST00000626147.1:n.461-167C=
ENST00000630721.1:c.308-167C=
NM_001042537.1:c.1728-167C= NP_001036002.1:n.1728-167C=
NM_001177651.1:c.1572-167C= NP_001171122.1:n.1572-167C=
NM_006359.2:c.1632-167C= NP_006350.1:n.1632-167C=
XM_006724726.2:c.1572-167C= XP_006724789.1:n.1572-167C=
XM_011531243.1:c.1476-167C= XP_011529545.1:n.1476-167C=
NM_001330652.1:c.1476-167C= NP_001317581.1:n.1476-167C=
XM_006724726.3:c.1572-167C= XP_006724789.1:n.1572-167C=
XM_017029223.2:c.1572-167C= XP_016884712.1:n.1572-167C=
XM_017029224.1:c.1572-167C= XP_016884713.1:n.1572-167C=
XM_017029225.1:c.1476-167C= XP_016884714.1:n.1476-167C=
NM_001177651.2:c.1572-167C= NP_001171122.1:n.1572-167C=
NM_001330652.2:c.1476-167C= NP_001317581.1:n.1476-167C=
NM_006359.3:c.1632-167C= NP_006350.1:n.1632-167C=
NM_001042537.2:c.1728-167C= NP_001036002.1:n.1728-167C=
NM_001379110.1:c.1662-167C= MANE Select NP_001366039.1:n.1662-167C=
NM_001400909.1:c.1572-167C= NP_001387838.1:n.1572-167C=
NM_001400910.1:c.1572-167C= NP_001387839.1:n.1572-167C=
NM_001400911.1:c.1572-167C= NP_001387840.1:n.1572-167C=
NM_001400912.1:c.1572-167C= NP_001387841.1:n.1572-167C=
NM_001400913.1:c.1476-167C= NP_001387842.1:n.1476-167C=
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