Canonical Allele Identifier: CA1207937237

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910361G= , CM000663.2:g.173910361G=	GRCh38
NC_000001.10:g.173879499G= , CM000663.1:g.173879499G=	GRCh37
NC_000001.9:g.172146122G=	NCBI36
NG_012462.1:g.12018C= , LRG_577:g.12018C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.762+393C= MANE Select	ENSP00000356671.3:n.762+393C=
ENST00000367698.3:c.762+393C=	ENSP00000356671.3:n.762+393C=
ENST00000487183.1:n.413+393C=
ENST00000617423.4:c.559+1503C=	ENSP00000478688.1:n.559+1503C=
NM_000488.3:c.762+393C= , LRG_577t1:c.762+393C=	NP_000479.1:n.762+393C=
XM_005245198.2:c.618+393C=	XP_005245255.1:n.618+393C=
NM_001365052.1:c.618+393C=	NP_001351981.1:n.618+393C=
NM_000488.4:c.762+393C= MANE Select	NP_000479.1:n.762+393C=
NM_001365052.2:c.618+393C=	NP_001351981.1:n.618+393C=
NM_001386302.1:c.885+270C=	NP_001373231.1:n.885+270C=
NM_001386303.1:c.843+393C=	NP_001373232.1:n.843+393C=
NM_001386304.1:c.741+414C=	NP_001373233.1:n.741+414C=
NM_001386305.1:c.762+393C=	NP_001373234.1:n.762+393C=
NM_001386306.1:c.546+393C=	NP_001373235.1:n.546+393C=