Canonical Allele Identifier: CA515624841

Gene: PIGA

Linked Data

• MyVariant Identifiers: chrX:g.15349593_15349594insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15331471_15331472insA , CM000685.2:g.15331471_15331472insA	GRCh38
NC_000023.10:g.15349593_15349594insA , CM000685.1:g.15349593_15349594insA	GRCh37
NC_000023.9:g.15259514_15259515insA	NCBI36
NG_009786.1:g.9067_9068insT , LRG_160:g.9067_9068insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333590.6:c.459_460insT MANE Select	ENSP00000369820.3:p.His154SerfsTer8
ENST00000637296.1:c.-314-173_-314-172insT	ENSP00000490545.1:n.-314-173_-314-172insT
ENST00000637626.1:c.459_460insT	ENSP00000489928.1:p.His154SerfsTer8
ENST00000638131.1:c.111+348_111+349insT	ENSP00000490483.1:n.111+348_111+349insT
ENST00000333590.5:c.459_460insT	ENSP00000369820.3:p.His154SerfsTer8
ENST00000474662.2:n.142+402_142+403insT
ENST00000482148.6:c.341+118_341+119insT	ENSP00000489528.1:n.341+118_341+119insT
ENST00000542278.6:c.459_460insT	ENSP00000442653.2:p.His154SerfsTer8
ENST00000634286.1:c.134+118_134+119insT	ENSP00000489491.1:n.134+118_134+119insT
ENST00000634582.1:c.13+4029_13+4030insT	ENSP00000489540.1:n.13+4029_13+4030insT
ENST00000634640.1:c.-231+402_-231+403insT	ENSP00000489083.1:n.-231+402_-231+403insT
ENST00000635045.1:n.544_545insT
ENST00000635598.1:c.341+118_341+119insT	ENSP00000489207.1:n.341+118_341+119insT
NM_002641.3:c.459_460insT , LRG_160t1:c.459_460insT	NP_002632.1:p.His154SerfsTer8
NM_020473.3:c.13+4029_13+4030insT	NP_065206.3:n.13+4029_13+4030insT
NR_033835.1:n.457+118_457+119insT
NR_033836.1:n.173+402_173+403insT
NM_002641.4:c.459_460insT MANE Select	NP_002632.1:p.His154SerfsTer8