Canonical Allele Identifier: CA1148224791

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909824C= , CM000663.2:g.173909824C=	GRCh38
NC_000001.10:g.173878962C= , CM000663.1:g.173878962C=	GRCh37
NC_000001.9:g.172145585C=	NCBI36
NG_012462.1:g.12555G= , LRG_577:g.12555G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.881G= MANE Select	ENSP00000356671.3:p.Arg294=
ENST00000367698.3:c.881G=	ENSP00000356671.3:p.Arg294=
ENST00000487183.1:n.532G=
ENST00000617423.4:c.559+2040G=	ENSP00000478688.1:n.559+2040G=
NM_000488.3:c.881G= , LRG_577t1:c.881G=	NP_000479.1:p.Arg294=
XM_005245198.2:c.737G=	XP_005245255.1:p.Arg246=
NM_001365052.1:c.737G=	NP_001351981.1:p.Arg246=
NM_000488.4:c.881G= MANE Select	NP_000479.1:p.Arg294=
NM_001365052.2:c.737G=	NP_001351981.1:p.Arg246=
NM_001386302.1:c.1004G=	NP_001373231.1:p.Arg335=
NM_001386303.1:c.962G=	NP_001373232.1:p.Arg321=
NM_001386304.1:c.860G=	NP_001373233.1:p.Arg287=
NM_001386305.1:c.824G=	NP_001373234.1:p.Arg275=
NM_001386306.1:c.665G=	NP_001373235.1:p.Arg222=