Canonical Allele Identifier: CA1207934361
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903911A= , CM000663.2:g.173903911A= GRCh38
NC_000001.10:g.173873049A= , CM000663.1:g.173873049A= GRCh37
NC_000001.9:g.172139672A= NCBI36
NG_012462.1:g.18468T= , LRG_577:g.18468T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1373T= MANE Select ENSP00000356671.3:p.Val458=
ENST00000367698.3:c.1373T= ENSP00000356671.3:p.Val458=
ENST00000617423.4:c.758T= ENSP00000478688.1:p.Val253=
NM_000488.3:c.1373T= , LRG_577t1:c.1373T= NP_000479.1:p.Val458=
XM_005245198.2:c.1229T= XP_005245255.1:p.Val410=
NM_001365052.1:c.1229T= NP_001351981.1:p.Val410=
NM_000488.4:c.1373T= MANE Select NP_000479.1:p.Val458=
NM_001365052.2:c.1229T= NP_001351981.1:p.Val410=
NM_001386302.1:c.1496T= NP_001373231.1:p.Val499=
NM_001386303.1:c.1454T= NP_001373232.1:p.Val485=
NM_001386304.1:c.1352T= NP_001373233.1:p.Val451=
NM_001386305.1:c.1316T= NP_001373234.1:p.Val439=
NM_001386306.1:c.1157T= NP_001373235.1:p.Val386=