Canonical Allele Identifier: CA2416904177

Gene: PIGA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15324670C= , CM000685.2:g.15324670C=	GRCh38
NC_000023.10:g.15342792C= , CM000685.1:g.15342792C=	GRCh37
NC_000023.9:g.15252713C=	NCBI36
NG_009786.1:g.15869G= , LRG_160:g.15869G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.1183G= MANE Select	ENSP00000369820.3:p.Glu395=
ENST00000637296.1:c.238G=	ENSP00000490545.1:p.Glu80=
ENST00000637626.1:c.*664G=	ENSP00000489928.1:n.*664G=
ENST00000638131.1:c.*444G=	ENSP00000490483.1:n.*444G=
ENST00000333590.5:c.1183G=	ENSP00000369820.3:p.Glu395=
ENST00000463173.1:n.455G=
ENST00000475746.1:c.81+350G=	ENSP00000488970.1:n.81+350G=
ENST00000482148.6:c.676G=	ENSP00000489528.1:p.Glu226=
ENST00000542278.6:c.1183G=	ENSP00000442653.2:p.Glu395=
ENST00000634582.1:c.481G=	ENSP00000489540.1:p.Glu161=
ENST00000634640.1:c.238G=	ENSP00000489083.1:p.Glu80=
ENST00000635045.1:n.1416G=
ENST00000635598.1:c.*452G=	ENSP00000489207.1:n.*452G=
ENST00000635631.1:n.524G=
NM_002641.3:c.1183G= , LRG_160t1:c.1183G=	NP_002632.1:p.Glu395=
NM_020473.3:c.481G=	NP_065206.3:p.Glu161=
NR_033835.1:n.925G=
NR_033836.1:n.641G=
XM_011545539.1:c.490G=	XP_011543841.1:p.Glu164=
XM_011545539.2:c.490G=	XP_011543841.1:p.Glu164=
NM_002641.4:c.1183G= MANE Select	NP_002632.1:p.Glu395=