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: CA2254349371
Gene: FOXN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28537074C= , CM000679.2:g.28537074C= GRCh38
NC_000017.10:g.26864092C= , CM000679.1:g.26864092C= GRCh37
NC_000017.9:g.23888219C= NCBI36
NG_007260.1:g.18134C= , LRG_61:g.18134C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000577936.2:c.1628-43C= ENSP00000462159.2:n.1628-43C=
ENST00000579795.6:c.1628-43C= MANE Select ENSP00000464645.1:n.1628-43C=
ENST00000226247.2:c.1628-43C= ENSP00000226247.2:n.1628-43C=
ENST00000481916.6:c.*1195+66977G= ENSP00000436369.2:n.*1195+66977G=
ENST00000579795.5:c.1628-43C= ENSP00000464645.1:n.1628-43C=
NM_003593.2:c.1628-43C= , LRG_61t1:c.1628-43C= NP_003584.2:n.1628-43C=
XM_005258046.3:c.1628-43C= XP_005258103.1:n.1628-43C=
XM_011525354.1:c.1685-43C= XP_011523656.1:n.1685-43C=
XM_011525355.1:c.1682-43C= XP_011523657.1:n.1682-43C=
XM_011525356.1:c.1682-43C= XP_011523658.1:n.1682-43C=
XM_011525357.1:c.1664-43C= XP_011523659.1:n.1664-43C=
XM_011525358.1:c.1631-43C= XP_011523660.1:n.1631-43C=
XM_011525359.1:c.1631-43C= XP_011523661.1:n.1631-43C=
XM_011525360.1:c.1631-43C= XP_011523662.1:n.1631-43C=
XM_011525361.1:c.1628-43C= XP_011523663.1:n.1628-43C=
XM_011525362.1:c.1628-43C= XP_011523664.1:n.1628-43C=
XM_011525363.1:c.1439-43C= XP_011523665.1:n.1439-43C=
XM_011525364.1:c.1163-43C= XP_011523666.1:n.1163-43C=
XM_011525365.1:c.1193-43C= XP_011523667.1:n.1193-43C=
XM_011525366.1:c.1085-43C= XP_011523668.1:n.1085-43C=
XM_011525367.1:c.1070-43C= XP_011523669.1:n.1070-43C=
XM_011525368.1:c.992-43C= XP_011523670.1:n.992-43C=
XM_011525369.1:c.992-43C= XP_011523671.1:n.992-43C=
XM_011525370.1:c.992-43C= XP_011523672.1:n.992-43C=
XM_011525368.2:c.992-43C= XP_011523670.1:n.992-43C=
XM_011525369.2:c.992-43C= XP_011523671.1:n.992-43C=
XM_011525370.2:c.992-43C= XP_011523672.1:n.992-43C=
XM_017025228.1:c.1628-43C= XP_016880717.1:n.1628-43C=
XM_017025229.1:c.1385-43C= XP_016880718.1:n.1385-43C=
XM_017025230.1:c.1139-43C= XP_016880719.1:n.1139-43C=
NM_001369369.1:c.1628-43C= MANE Select NP_001356298.1:n.1628-43C=
NM_003593.3:c.1628-43C= NP_003584.2:n.1628-43C=