Canonical Allele Identifier: CA1207936990

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909770G= , CM000663.2:g.173909770G=	GRCh38
NC_000001.10:g.173878908G= , CM000663.1:g.173878908G=	GRCh37
NC_000001.9:g.172145531G=	NCBI36
NG_012462.1:g.12609C= , LRG_577:g.12609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.935C= MANE Select	ENSP00000356671.3:p.Thr312=
ENST00000367698.3:c.935C=	ENSP00000356671.3:p.Thr312=
ENST00000487183.1:n.586C=
ENST00000617423.4:c.559+2094C=	ENSP00000478688.1:n.559+2094C=
NM_000488.3:c.935C= , LRG_577t1:c.935C=	NP_000479.1:p.Thr312=
XM_005245198.2:c.791C=	XP_005245255.1:p.Thr264=
NM_001365052.1:c.791C=	NP_001351981.1:p.Thr264=
NM_000488.4:c.935C= MANE Select	NP_000479.1:p.Thr312=
NM_001365052.2:c.791C=	NP_001351981.1:p.Thr264=
NM_001386302.1:c.1058C=	NP_001373231.1:p.Thr353=
NM_001386303.1:c.1016C=	NP_001373232.1:p.Thr339=
NM_001386304.1:c.914C=	NP_001373233.1:p.Thr305=
NM_001386305.1:c.878C=	NP_001373234.1:p.Thr293=
NM_001386306.1:c.719C=	NP_001373235.1:p.Thr240=