Canonical Allele Identifier: CA1207937243

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910377G= , CM000663.2:g.173910377G=	GRCh38
NC_000001.10:g.173879515G= , CM000663.1:g.173879515G=	GRCh37
NC_000001.9:g.172146138G=	NCBI36
NG_012462.1:g.12002C= , LRG_577:g.12002C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.762+377C= MANE Select	ENSP00000356671.3:n.762+377C=
ENST00000367698.3:c.762+377C=	ENSP00000356671.3:n.762+377C=
ENST00000487183.1:n.413+377C=
ENST00000617423.4:c.559+1487C=	ENSP00000478688.1:n.559+1487C=
NM_000488.3:c.762+377C= , LRG_577t1:c.762+377C=	NP_000479.1:n.762+377C=
XM_005245198.2:c.618+377C=	XP_005245255.1:n.618+377C=
NM_001365052.1:c.618+377C=	NP_001351981.1:n.618+377C=
NM_000488.4:c.762+377C= MANE Select	NP_000479.1:n.762+377C=
NM_001365052.2:c.618+377C=	NP_001351981.1:n.618+377C=
NM_001386302.1:c.885+254C=	NP_001373231.1:n.885+254C=
NM_001386303.1:c.843+377C=	NP_001373232.1:n.843+377C=
NM_001386304.1:c.741+398C=	NP_001373233.1:n.741+398C=
NM_001386305.1:c.762+377C=	NP_001373234.1:n.762+377C=
NM_001386306.1:c.546+377C=	NP_001373235.1:n.546+377C=