Canonical Allele Identifier: CA412339716

Gene: PIGA

Linked Data

• MyVariant Identifiers: chrX:g.15349590A>G (hg19) ; chrX:g.15331468A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331468A>G , CM000685.2:g.15331468A>G	GRCh38
NC_000023.10:g.15349590A>G , CM000685.1:g.15349590A>G	GRCh37
NC_000023.9:g.15259511A>G	NCBI36
NG_009786.1:g.9071T>C , LRG_160:g.9071T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.463T>C MANE Select	ENSP00000369820.3:p.Ser155Pro
ENST00000637296.1:c.-314-169T>C	ENSP00000490545.1:n.-314-169T>C
ENST00000637626.1:c.463T>C	ENSP00000489928.1:p.Ser155Pro
ENST00000638131.1:c.111+352T>C	ENSP00000490483.1:n.111+352T>C
ENST00000333590.5:c.463T>C	ENSP00000369820.3:p.Ser155Pro
ENST00000474662.2:n.142+406T>C
ENST00000482148.6:c.341+122T>C	ENSP00000489528.1:n.341+122T>C
ENST00000542278.6:c.463T>C	ENSP00000442653.2:p.Ser155Pro
ENST00000634286.1:c.134+122T>C	ENSP00000489491.1:n.134+122T>C
ENST00000634582.1:c.13+4033T>C	ENSP00000489540.1:n.13+4033T>C
ENST00000634640.1:c.-231+406T>C	ENSP00000489083.1:n.-231+406T>C
ENST00000635045.1:n.548T>C
ENST00000635598.1:c.341+122T>C	ENSP00000489207.1:n.341+122T>C
NM_002641.3:c.463T>C , LRG_160t1:c.463T>C	NP_002632.1:p.Ser155Pro
NM_020473.3:c.13+4033T>C	NP_065206.3:n.13+4033T>C
NR_033835.1:n.457+122T>C
NR_033836.1:n.173+406T>C
NM_002641.4:c.463T>C MANE Select	NP_002632.1:p.Ser155Pro