Canonical Allele Identifier: CA1207936961
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909720T= , CM000663.2:g.173909720T= GRCh38
NC_000001.10:g.173878858T= , CM000663.1:g.173878858T= GRCh37
NC_000001.9:g.172145481T= NCBI36
NG_012462.1:g.12659A= , LRG_577:g.12659A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.985A= MANE Select ENSP00000356671.3:p.Lys329=
ENST00000367698.3:c.985A= ENSP00000356671.3:p.Lys329=
ENST00000617423.4:c.559+2144A= ENSP00000478688.1:n.559+2144A=
NM_000488.3:c.985A= , LRG_577t1:c.985A= NP_000479.1:p.Lys329=
XM_005245198.2:c.841A= XP_005245255.1:p.Lys281=
NM_001365052.1:c.841A= NP_001351981.1:p.Lys281=
NM_000488.4:c.985A= MANE Select NP_000479.1:p.Lys329=
NM_001365052.2:c.841A= NP_001351981.1:p.Lys281=
NM_001386302.1:c.1108A= NP_001373231.1:p.Lys370=
NM_001386303.1:c.1066A= NP_001373232.1:p.Lys356=
NM_001386304.1:c.964A= NP_001373233.1:p.Lys322=
NM_001386305.1:c.928A= NP_001373234.1:p.Lys310=
NM_001386306.1:c.769A= NP_001373235.1:p.Lys257=