Canonical Allele Identifier: CA412340695

Gene: PIGA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331638T>G , CM000685.2:g.15331638T>G	GRCh38
NC_000023.10:g.15349760T>G , CM000685.1:g.15349760T>G	GRCh37
NC_000023.9:g.15259681T>G	NCBI36
NG_009786.1:g.8901A>C , LRG_160:g.8901A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.293A>C MANE Select	ENSP00000369820.3:p.Tyr98Ser
ENST00000637296.1:c.-315+236A>C	ENSP00000490545.1:n.-315+236A>C
ENST00000637626.1:c.293A>C	ENSP00000489928.1:p.Tyr98Ser
ENST00000638131.1:c.111+182A>C	ENSP00000490483.1:n.111+182A>C
ENST00000333590.5:c.293A>C	ENSP00000369820.3:p.Tyr98Ser
ENST00000474662.2:n.142+236A>C
ENST00000482148.6:c.293A>C	ENSP00000489528.1:p.Tyr98Ser
ENST00000542278.6:c.293A>C	ENSP00000442653.2:p.Tyr98Ser
ENST00000634286.1:c.86A>C	ENSP00000489491.1:p.Tyr29Ser
ENST00000634582.1:c.13+3863A>C	ENSP00000489540.1:n.13+3863A>C
ENST00000634640.1:c.-231+236A>C	ENSP00000489083.1:n.-231+236A>C
ENST00000635045.1:n.378A>C
ENST00000635543.1:c.293A>C	ENSP00000489205.1:p.Tyr98Ser
ENST00000635598.1:c.293A>C	ENSP00000489207.1:p.Tyr98Ser
NM_002641.3:c.293A>C , LRG_160t1:c.293A>C	NP_002632.1:p.Tyr98Ser
NM_020473.3:c.13+3863A>C	NP_065206.3:n.13+3863A>C
NR_033835.1:n.409A>C
NR_033836.1:n.173+236A>C
NM_002641.4:c.293A>C MANE Select	NP_002632.1:p.Tyr98Ser