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: CA1207936486
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173908584_173908585delinsAG , CM000663.2:g.173908584_173908585delinsAG GRCh38
NC_000001.10:g.173877722_173877723delinsAG , CM000663.1:g.173877722_173877723delinsAG GRCh37
NC_000001.9:g.172144345_172144346delinsAG NCBI36
NG_012462.1:g.13794_13795delinsCT , LRG_577:g.13794_13795delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1153+967_1153+968delinsCT MANE Select ENSP00000356671.3:n.1153+967_1153+968delinsCT
ENST00000367698.3:c.1153+967_1153+968delinsCT ENSP00000356671.3:n.1153+967_1153+968delinsCT
ENST00000617423.4:c.560-1092_560-1091delinsCT ENSP00000478688.1:n.560-1092_560-1091delinsCT
NM_000488.3:c.1153+967_1153+968delinsCT , LRG_577t1:c.1153+967_1153+968delinsCT NP_000479.1:n.1153+967_1153+968delinsCT
XM_005245198.2:c.1009+967_1009+968delinsCT XP_005245255.1:n.1009+967_1009+968delinsCT
NM_001365052.1:c.1009+967_1009+968delinsCT NP_001351981.1:n.1009+967_1009+968delinsCT
NM_000488.4:c.1153+967_1153+968delinsCT MANE Select NP_000479.1:n.1153+967_1153+968delinsCT
NM_001365052.2:c.1009+967_1009+968delinsCT NP_001351981.1:n.1009+967_1009+968delinsCT
NM_001386302.1:c.1276+967_1276+968delinsCT NP_001373231.1:n.1276+967_1276+968delinsCT
NM_001386303.1:c.1234+967_1234+968delinsCT NP_001373232.1:n.1234+967_1234+968delinsCT
NM_001386304.1:c.1132+967_1132+968delinsCT NP_001373233.1:n.1132+967_1132+968delinsCT
NM_001386305.1:c.1096+967_1096+968delinsCT NP_001373234.1:n.1096+967_1096+968delinsCT
NM_001386306.1:c.937+967_937+968delinsCT NP_001373235.1:n.937+967_937+968delinsCT
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