Canonical Allele Identifier: CA1207936975

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909744C= , CM000663.2:g.173909744C=	GRCh38
NC_000001.10:g.173878882C= , CM000663.1:g.173878882C=	GRCh37
NC_000001.9:g.172145505C=	NCBI36
NG_012462.1:g.12635G= , LRG_577:g.12635G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.961G= MANE Select	ENSP00000356671.3:p.Glu321=
ENST00000367698.3:c.961G=	ENSP00000356671.3:p.Glu321=
ENST00000487183.1:n.612G=
ENST00000617423.4:c.559+2120G=	ENSP00000478688.1:n.559+2120G=
NM_000488.3:c.961G= , LRG_577t1:c.961G=	NP_000479.1:p.Glu321=
XM_005245198.2:c.817G=	XP_005245255.1:p.Glu273=
NM_001365052.1:c.817G=	NP_001351981.1:p.Glu273=
NM_000488.4:c.961G= MANE Select	NP_000479.1:p.Glu321=
NM_001365052.2:c.817G=	NP_001351981.1:p.Glu273=
NM_001386302.1:c.1084G=	NP_001373231.1:p.Glu362=
NM_001386303.1:c.1042G=	NP_001373232.1:p.Glu348=
NM_001386304.1:c.940G=	NP_001373233.1:p.Glu314=
NM_001386305.1:c.904G=	NP_001373234.1:p.Glu302=
NM_001386306.1:c.745G=	NP_001373235.1:p.Glu249=