Canonical Allele Identifier: CA1207936993

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909784T= , CM000663.2:g.173909784T=	GRCh38
NC_000001.10:g.173878922T= , CM000663.1:g.173878922T=	GRCh37
NC_000001.9:g.172145545T=	NCBI36
NG_012462.1:g.12595A= , LRG_577:g.12595A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.921A= MANE Select	ENSP00000356671.3:p.Lys307=
ENST00000367698.3:c.921A=	ENSP00000356671.3:p.Lys307=
ENST00000487183.1:n.572A=
ENST00000617423.4:c.559+2080A=	ENSP00000478688.1:n.559+2080A=
NM_000488.3:c.921A= , LRG_577t1:c.921A=	NP_000479.1:p.Lys307=
XM_005245198.2:c.777A=	XP_005245255.1:p.Lys259=
NM_001365052.1:c.777A=	NP_001351981.1:p.Lys259=
NM_000488.4:c.921A= MANE Select	NP_000479.1:p.Lys307=
NM_001365052.2:c.777A=	NP_001351981.1:p.Lys259=
NM_001386302.1:c.1044A=	NP_001373231.1:p.Lys348=
NM_001386303.1:c.1002A=	NP_001373232.1:p.Lys334=
NM_001386304.1:c.900A=	NP_001373233.1:p.Lys300=
NM_001386305.1:c.864A=	NP_001373234.1:p.Lys288=
NM_001386306.1:c.705A=	NP_001373235.1:p.Lys235=