Canonical Allele Identifier: CA2416906315

Gene: PIGA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331645C= , CM000685.2:g.15331645C=	GRCh38
NC_000023.10:g.15349767C= , CM000685.1:g.15349767C=	GRCh37
NC_000023.9:g.15259688C=	NCBI36
NG_009786.1:g.8894G= , LRG_160:g.8894G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.286G= MANE Select	ENSP00000369820.3:p.Val96=
ENST00000637296.1:c.-315+229G=	ENSP00000490545.1:n.-315+229G=
ENST00000637626.1:c.286G=	ENSP00000489928.1:p.Val96=
ENST00000638131.1:c.111+175G=	ENSP00000490483.1:n.111+175G=
ENST00000333590.5:c.286G=	ENSP00000369820.3:p.Val96=
ENST00000474662.2:n.142+229G=
ENST00000482148.6:c.286G=	ENSP00000489528.1:p.Val96=
ENST00000542278.6:c.286G=	ENSP00000442653.2:p.Val96=
ENST00000634286.1:c.79G=	ENSP00000489491.1:p.Val27=
ENST00000634582.1:c.13+3856G=	ENSP00000489540.1:n.13+3856G=
ENST00000634640.1:c.-231+229G=	ENSP00000489083.1:n.-231+229G=
ENST00000635045.1:n.371G=
ENST00000635543.1:c.286G=	ENSP00000489205.1:p.Val96=
ENST00000635598.1:c.286G=	ENSP00000489207.1:p.Val96=
NM_002641.3:c.286G= , LRG_160t1:c.286G=	NP_002632.1:p.Val96=
NM_020473.3:c.13+3856G=	NP_065206.3:n.13+3856G=
NR_033835.1:n.402G=
NR_033836.1:n.173+229G=
NM_002641.4:c.286G= MANE Select	NP_002632.1:p.Val96=