Canonical Allele Identifier: CA412339903

Gene: PIGA

Linked Data

• COSMIC: COSM242598
• MyVariant Identifiers: chrX:g.15349616C>A (hg19) ; chrX:g.15331494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331494C>A , CM000685.2:g.15331494C>A	GRCh38
NC_000023.10:g.15349616C>A , CM000685.1:g.15349616C>A	GRCh37
NC_000023.9:g.15259537C>A	NCBI36
NG_009786.1:g.9045G>T , LRG_160:g.9045G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.437G>T MANE Select	ENSP00000369820.3:p.Gly146Val
ENST00000637296.1:c.-314-195G>T	ENSP00000490545.1:n.-314-195G>T
ENST00000637626.1:c.437G>T	ENSP00000489928.1:p.Gly146Val
ENST00000638131.1:c.111+326G>T	ENSP00000490483.1:n.111+326G>T
ENST00000333590.5:c.437G>T	ENSP00000369820.3:p.Gly146Val
ENST00000474662.2:n.142+380G>T
ENST00000482148.6:c.341+96G>T	ENSP00000489528.1:n.341+96G>T
ENST00000542278.6:c.437G>T	ENSP00000442653.2:p.Gly146Val
ENST00000634286.1:c.134+96G>T	ENSP00000489491.1:n.134+96G>T
ENST00000634582.1:c.13+4007G>T	ENSP00000489540.1:n.13+4007G>T
ENST00000634640.1:c.-231+380G>T	ENSP00000489083.1:n.-231+380G>T
ENST00000635045.1:n.522G>T
ENST00000635543.1:c.437G>T	ENSP00000489205.1:p.Gly146Val
ENST00000635598.1:c.341+96G>T	ENSP00000489207.1:n.341+96G>T
NM_002641.3:c.437G>T , LRG_160t1:c.437G>T	NP_002632.1:p.Gly146Val
NM_020473.3:c.13+4007G>T	NP_065206.3:n.13+4007G>T
NR_033835.1:n.457+96G>T
NR_033836.1:n.173+380G>T
NM_002641.4:c.437G>T MANE Select	NP_002632.1:p.Gly146Val