Canonical Allele Identifier: CA1143355584

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911933G= , CM000663.2:g.173911933G=	GRCh38
NC_000001.10:g.173881071G= , CM000663.1:g.173881071G=	GRCh37
NC_000001.9:g.172147694G=	NCBI36
NG_012462.1:g.10446C= , LRG_577:g.10446C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.490C= MANE Select	ENSP00000356671.3:p.Arg164=
ENST00000367698.3:c.490C=	ENSP00000356671.3:p.Arg164=
ENST00000487183.1:n.195C=
ENST00000617423.4:c.490C=	ENSP00000478688.1:p.Arg164=
NM_000488.3:c.490C= , LRG_577t1:c.490C=	NP_000479.1:p.Arg164=
XM_005245198.2:c.346C=	XP_005245255.1:p.Arg116=
NM_001365052.1:c.346C=	NP_001351981.1:p.Arg116=
NM_000488.4:c.490C= MANE Select	NP_000479.1:p.Arg164=
NM_001365052.2:c.346C=	NP_001351981.1:p.Arg116=
NM_001386302.1:c.490C=	NP_001373231.1:p.Arg164=
NM_001386303.1:c.571C=	NP_001373232.1:p.Arg191=
NM_001386304.1:c.490C=	NP_001373233.1:p.Arg164=
NM_001386305.1:c.490C=	NP_001373234.1:p.Arg164=
NM_001386306.1:c.409-1042C=	NP_001373235.1:n.409-1042C=