Canonical Allele Identifier: CA1207936923

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909635A= , CM000663.2:g.173909635A=	GRCh38
NC_000001.10:g.173878773A= , CM000663.1:g.173878773A=	GRCh37
NC_000001.9:g.172145396A=	NCBI36
NG_012462.1:g.12744T= , LRG_577:g.12744T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1070T= MANE Select	ENSP00000356671.3:p.Ile357=
ENST00000367698.3:c.1070T=	ENSP00000356671.3:p.Ile357=
ENST00000617423.4:c.560-2142T=	ENSP00000478688.1:n.560-2142T=
NM_000488.3:c.1070T= , LRG_577t1:c.1070T=	NP_000479.1:p.Ile357=
XM_005245198.2:c.926T=	XP_005245255.1:p.Ile309=
NM_001365052.1:c.926T=	NP_001351981.1:p.Ile309=
NM_000488.4:c.1070T= MANE Select	NP_000479.1:p.Ile357=
NM_001365052.2:c.926T=	NP_001351981.1:p.Ile309=
NM_001386302.1:c.1193T=	NP_001373231.1:p.Ile398=
NM_001386303.1:c.1151T=	NP_001373232.1:p.Ile384=
NM_001386304.1:c.1049T=	NP_001373233.1:p.Ile350=
NM_001386305.1:c.1013T=	NP_001373234.1:p.Ile338=
NM_001386306.1:c.854T=	NP_001373235.1:p.Ile285=