Canonical Allele Identifier: CA412340810

Gene: PIGA

Linked Data

• ClinVar Variation Id: 2050896
• ClinVar RCV Id: RCV002904676
• MyVariant Identifiers: chrX:g.15349781T>C (hg19) ; chrX:g.15331659T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331659T>C , CM000685.2:g.15331659T>C	GRCh38
NC_000023.10:g.15349781T>C , CM000685.1:g.15349781T>C	GRCh37
NC_000023.9:g.15259702T>C	NCBI36
NG_009786.1:g.8880A>G , LRG_160:g.8880A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.272A>G MANE Select	ENSP00000369820.3:p.Tyr91Cys
ENST00000637296.1:c.-315+215A>G	ENSP00000490545.1:n.-315+215A>G
ENST00000637626.1:c.272A>G	ENSP00000489928.1:p.Tyr91Cys
ENST00000638131.1:c.111+161A>G	ENSP00000490483.1:n.111+161A>G
ENST00000333590.5:c.272A>G	ENSP00000369820.3:p.Tyr91Cys
ENST00000474662.2:n.142+215A>G
ENST00000482148.6:c.272A>G	ENSP00000489528.1:p.Tyr91Cys
ENST00000542278.6:c.272A>G	ENSP00000442653.2:p.Tyr91Cys
ENST00000634286.1:c.65A>G	ENSP00000489491.1:p.Tyr22Cys
ENST00000634582.1:c.13+3842A>G	ENSP00000489540.1:n.13+3842A>G
ENST00000634640.1:c.-231+215A>G	ENSP00000489083.1:n.-231+215A>G
ENST00000635045.1:n.357A>G
ENST00000635543.1:c.272A>G	ENSP00000489205.1:p.Tyr91Cys
ENST00000635598.1:c.272A>G	ENSP00000489207.1:p.Tyr91Cys
NM_002641.3:c.272A>G , LRG_160t1:c.272A>G	NP_002632.1:p.Tyr91Cys
NM_020473.3:c.13+3842A>G	NP_065206.3:n.13+3842A>G
NR_033835.1:n.388A>G
NR_033836.1:n.173+215A>G
NM_002641.4:c.272A>G MANE Select	NP_002632.1:p.Tyr91Cys