Canonical Allele Identifier: CA1207934388

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904019A= , CM000663.2:g.173904019A=	GRCh38
NC_000001.10:g.173873157A= , CM000663.1:g.173873157A=	GRCh37
NC_000001.9:g.172139780A=	NCBI36
NG_012462.1:g.18360T= , LRG_577:g.18360T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1265T= MANE Select	ENSP00000356671.3:p.Ile422=
ENST00000367698.3:c.1265T=	ENSP00000356671.3:p.Ile422=
ENST00000617423.4:c.650T=	ENSP00000478688.1:p.Ile217=
NM_000488.3:c.1265T= , LRG_577t1:c.1265T=	NP_000479.1:p.Ile422=
XM_005245198.2:c.1121T=	XP_005245255.1:p.Ile374=
NM_001365052.1:c.1121T=	NP_001351981.1:p.Ile374=
NM_000488.4:c.1265T= MANE Select	NP_000479.1:p.Ile422=
NM_001365052.2:c.1121T=	NP_001351981.1:p.Ile374=
NM_001386302.1:c.1388T=	NP_001373231.1:p.Ile463=
NM_001386303.1:c.1346T=	NP_001373232.1:p.Ile449=
NM_001386304.1:c.1244T=	NP_001373233.1:p.Ile415=
NM_001386305.1:c.1208T=	NP_001373234.1:p.Ile403=
NM_001386306.1:c.1049T=	NP_001373235.1:p.Ile350=