Canonical Allele Identifier: CA1207936989

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909769G= , CM000663.2:g.173909769G=	GRCh38
NC_000001.10:g.173878907G= , CM000663.1:g.173878907G=	GRCh37
NC_000001.9:g.172145530G=	NCBI36
NG_012462.1:g.12610C= , LRG_577:g.12610C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.936C= MANE Select	ENSP00000356671.3:p.Thr312=
ENST00000367698.3:c.936C=	ENSP00000356671.3:p.Thr312=
ENST00000487183.1:n.587C=
ENST00000617423.4:c.559+2095C=	ENSP00000478688.1:n.559+2095C=
NM_000488.3:c.936C= , LRG_577t1:c.936C=	NP_000479.1:p.Thr312=
XM_005245198.2:c.792C=	XP_005245255.1:p.Thr264=
NM_001365052.1:c.792C=	NP_001351981.1:p.Thr264=
NM_000488.4:c.936C= MANE Select	NP_000479.1:p.Thr312=
NM_001365052.2:c.792C=	NP_001351981.1:p.Thr264=
NM_001386302.1:c.1059C=	NP_001373231.1:p.Thr353=
NM_001386303.1:c.1017C=	NP_001373232.1:p.Thr339=
NM_001386304.1:c.915C=	NP_001373233.1:p.Thr305=
NM_001386305.1:c.879C=	NP_001373234.1:p.Thr293=
NM_001386306.1:c.720C=	NP_001373235.1:p.Thr240=