Canonical Allele Identifier: CA1207938965

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914724A= , CM000663.2:g.173914724A=	GRCh38
NC_000001.10:g.173883862A= , CM000663.1:g.173883862A=	GRCh37
NC_000001.9:g.172150485A=	NCBI36
NG_012462.1:g.7655T= , LRG_577:g.7655T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.237T= MANE Select	ENSP00000356671.3:p.Arg79=
ENST00000367698.3:c.237T=	ENSP00000356671.3:p.Arg79=
ENST00000494024.1:n.463T=
ENST00000617423.4:c.237T=	ENSP00000478688.1:p.Arg79=
NM_000488.3:c.237T= , LRG_577t1:c.237T=	NP_000479.1:p.Arg79=
XM_005245198.2:c.93T=	XP_005245255.1:p.Arg31=
NM_001365052.1:c.93T=	NP_001351981.1:p.Arg31=
NM_000488.4:c.237T= MANE Select	NP_000479.1:p.Arg79=
NM_001365052.2:c.93T=	NP_001351981.1:p.Arg31=
NM_001386302.1:c.237T=	NP_001373231.1:p.Arg79=
NM_001386303.1:c.318T=	NP_001373232.1:p.Arg106=
NM_001386304.1:c.237T=	NP_001373233.1:p.Arg79=
NM_001386305.1:c.237T=	NP_001373234.1:p.Arg79=
NM_001386306.1:c.237T=	NP_001373235.1:p.Arg79=