Canonical Allele Identifier: CA1207938955

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914687T= , CM000663.2:g.173914687T=	GRCh38
NC_000001.10:g.173883825T= , CM000663.1:g.173883825T=	GRCh37
NC_000001.9:g.172150448T=	NCBI36
NG_012462.1:g.7692A= , LRG_577:g.7692A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.274A= MANE Select	ENSP00000356671.3:p.Thr92=
ENST00000367698.3:c.274A=	ENSP00000356671.3:p.Thr92=
ENST00000494024.1:n.500A=
ENST00000617423.4:c.274A=	ENSP00000478688.1:p.Thr92=
NM_000488.3:c.274A= , LRG_577t1:c.274A=	NP_000479.1:p.Thr92=
XM_005245198.2:c.130A=	XP_005245255.1:p.Thr44=
NM_001365052.1:c.130A=	NP_001351981.1:p.Thr44=
NM_000488.4:c.274A= MANE Select	NP_000479.1:p.Thr92=
NM_001365052.2:c.130A=	NP_001351981.1:p.Thr44=
NM_001386302.1:c.274A=	NP_001373231.1:p.Thr92=
NM_001386303.1:c.355A=	NP_001373232.1:p.Thr119=
NM_001386304.1:c.274A=	NP_001373233.1:p.Thr92=
NM_001386305.1:c.274A=	NP_001373234.1:p.Thr92=
NM_001386306.1:c.274A=	NP_001373235.1:p.Thr92=