Canonical Allele Identifier: CA2416906276
Gene: PIGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.15331487C= , CM000685.2:g.15331487C= GRCh38
NC_000023.10:g.15349609C= , CM000685.1:g.15349609C= GRCh37
NC_000023.9:g.15259530C= NCBI36
NG_009786.1:g.9052G= , LRG_160:g.9052G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333590.6:c.444G= MANE Select ENSP00000369820.3:p.Gln148=
ENST00000637296.1:c.-314-188G= ENSP00000490545.1:n.-314-188G=
ENST00000637626.1:c.444G= ENSP00000489928.1:p.Gln148=
ENST00000638131.1:c.111+333G= ENSP00000490483.1:n.111+333G=
ENST00000333590.5:c.444G= ENSP00000369820.3:p.Gln148=
ENST00000474662.2:n.142+387G=
ENST00000482148.6:c.341+103G= ENSP00000489528.1:n.341+103G=
ENST00000542278.6:c.444G= ENSP00000442653.2:p.Gln148=
ENST00000634286.1:c.134+103G= ENSP00000489491.1:n.134+103G=
ENST00000634582.1:c.13+4014G= ENSP00000489540.1:n.13+4014G=
ENST00000634640.1:c.-231+387G= ENSP00000489083.1:n.-231+387G=
ENST00000635045.1:n.529G=
ENST00000635543.1:c.444G= ENSP00000489205.1:p.Gln148=
ENST00000635598.1:c.341+103G= ENSP00000489207.1:n.341+103G=
NM_002641.3:c.444G= , LRG_160t1:c.444G= NP_002632.1:p.Gln148=
NM_020473.3:c.13+4014G= NP_065206.3:n.13+4014G=
NR_033835.1:n.457+103G=
NR_033836.1:n.173+387G=
NM_002641.4:c.444G= MANE Select NP_002632.1:p.Gln148=