Canonical Allele Identifier: CA1207937022

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909854A= , CM000663.2:g.173909854A=	GRCh38
NC_000001.10:g.173878992A= , CM000663.1:g.173878992A=	GRCh37
NC_000001.9:g.172145615A=	NCBI36
NG_012462.1:g.12525T= , LRG_577:g.12525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.851T= MANE Select	ENSP00000356671.3:p.Met284=
ENST00000367698.3:c.851T=	ENSP00000356671.3:p.Met284=
ENST00000487183.1:n.502T=
ENST00000617423.4:c.559+2010T=	ENSP00000478688.1:n.559+2010T=
NM_000488.3:c.851T= , LRG_577t1:c.851T=	NP_000479.1:p.Met284=
XM_005245198.2:c.707T=	XP_005245255.1:p.Met236=
NM_001365052.1:c.707T=	NP_001351981.1:p.Met236=
NM_000488.4:c.851T= MANE Select	NP_000479.1:p.Met284=
NM_001365052.2:c.707T=	NP_001351981.1:p.Met236=
NM_001386302.1:c.974T=	NP_001373231.1:p.Met325=
NM_001386303.1:c.932T=	NP_001373232.1:p.Met311=
NM_001386304.1:c.830T=	NP_001373233.1:p.Met277=
NM_001386305.1:c.794T=	NP_001373234.1:p.Met265=
NM_001386306.1:c.635T=	NP_001373235.1:p.Met212=