Canonical Allele Identifier: CA1207934359
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903894T= , CM000663.2:g.173903894T= GRCh38
NC_000001.10:g.173873032T= , CM000663.1:g.173873032T= GRCh37
NC_000001.9:g.172139655T= NCBI36
NG_012462.1:g.18485A= , LRG_577:g.18485A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1390A= MANE Select ENSP00000356671.3:p.Lys464=
ENST00000367698.3:c.1390A= ENSP00000356671.3:p.Lys464=
ENST00000617423.4:c.775A= ENSP00000478688.1:p.Lys259=
NM_000488.3:c.1390A= , LRG_577t1:c.1390A= NP_000479.1:p.Lys464=
XM_005245198.2:c.1246A= XP_005245255.1:p.Lys416=
NM_001365052.1:c.1246A= NP_001351981.1:p.Lys416=
NM_000488.4:c.1390A= MANE Select NP_000479.1:p.Lys464=
NM_001365052.2:c.1246A= NP_001351981.1:p.Lys416=
NM_001386302.1:c.1513A= NP_001373231.1:p.Lys505=
NM_001386303.1:c.1471A= NP_001373232.1:p.Lys491=
NM_001386304.1:c.1369A= NP_001373233.1:p.Lys457=
NM_001386305.1:c.1333A= NP_001373234.1:p.Lys445=
NM_001386306.1:c.1174A= NP_001373235.1:p.Lys392=