Canonical Allele Identifier: CA1207936903

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909592G= , CM000663.2:g.173909592G=	GRCh38
NC_000001.10:g.173878730G= , CM000663.1:g.173878730G=	GRCh37
NC_000001.9:g.172145353G=	NCBI36
NG_012462.1:g.12787C= , LRG_577:g.12787C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1113C= MANE Select	ENSP00000356671.3:p.Gly371=
ENST00000367698.3:c.1113C=	ENSP00000356671.3:p.Gly371=
ENST00000617423.4:c.560-2099C=	ENSP00000478688.1:n.560-2099C=
NM_000488.3:c.1113C= , LRG_577t1:c.1113C=	NP_000479.1:p.Gly371=
XM_005245198.2:c.969C=	XP_005245255.1:p.Gly323=
NM_001365052.1:c.969C=	NP_001351981.1:p.Gly323=
NM_000488.4:c.1113C= MANE Select	NP_000479.1:p.Gly371=
NM_001365052.2:c.969C=	NP_001351981.1:p.Gly323=
NM_001386302.1:c.1236C=	NP_001373231.1:p.Gly412=
NM_001386303.1:c.1194C=	NP_001373232.1:p.Gly398=
NM_001386304.1:c.1092C=	NP_001373233.1:p.Gly364=
NM_001386305.1:c.1056C=	NP_001373234.1:p.Gly352=
NM_001386306.1:c.897C=	NP_001373235.1:p.Gly299=