Canonical Allele Identifier: CA2416906244

Gene: PIGA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331315T= , CM000685.2:g.15331315T=	GRCh38
NC_000023.10:g.15349437T= , CM000685.1:g.15349437T=	GRCh37
NC_000023.9:g.15259358T=	NCBI36
NG_009786.1:g.9224A= , LRG_160:g.9224A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.616A= MANE Select	ENSP00000369820.3:p.Ile206=
ENST00000637296.1:c.-314-16A=	ENSP00000490545.1:n.-314-16A=
ENST00000637626.1:c.616A=	ENSP00000489928.1:p.Ile206=
ENST00000638131.1:c.111+505A=	ENSP00000490483.1:n.111+505A=
ENST00000333590.5:c.616A=	ENSP00000369820.3:p.Ile206=
ENST00000474662.2:n.142+559A=
ENST00000482148.6:c.341+275A=	ENSP00000489528.1:n.341+275A=
ENST00000542278.6:c.616A=	ENSP00000442653.2:p.Ile206=
ENST00000634286.1:c.134+275A=	ENSP00000489491.1:n.134+275A=
ENST00000634582.1:c.13+4186A=	ENSP00000489540.1:n.13+4186A=
ENST00000634640.1:c.-231+559A=	ENSP00000489083.1:n.-231+559A=
ENST00000635045.1:n.701A=
ENST00000635598.1:c.341+275A=	ENSP00000489207.1:n.341+275A=
NM_002641.3:c.616A= , LRG_160t1:c.616A=	NP_002632.1:p.Ile206=
NM_020473.3:c.13+4186A=	NP_065206.3:n.13+4186A=
NR_033835.1:n.457+275A=
NR_033836.1:n.173+559A=
NM_002641.4:c.616A= MANE Select	NP_002632.1:p.Ile206=