Canonical Allele Identifier: CA2416906287
Gene: PIGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.15331531T= , CM000685.2:g.15331531T= GRCh38
NC_000023.10:g.15349653T= , CM000685.1:g.15349653T= GRCh37
NC_000023.9:g.15259574T= NCBI36
NG_009786.1:g.9008A= , LRG_160:g.9008A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333590.6:c.400A= MANE Select ENSP00000369820.3:p.Met134=
ENST00000637296.1:c.-314-232A= ENSP00000490545.1:n.-314-232A=
ENST00000637626.1:c.400A= ENSP00000489928.1:p.Met134=
ENST00000638131.1:c.111+289A= ENSP00000490483.1:n.111+289A=
ENST00000333590.5:c.400A= ENSP00000369820.3:p.Met134=
ENST00000474662.2:n.142+343A=
ENST00000482148.6:c.341+59A= ENSP00000489528.1:n.341+59A=
ENST00000542278.6:c.400A= ENSP00000442653.2:p.Met134=
ENST00000634286.1:c.134+59A= ENSP00000489491.1:n.134+59A=
ENST00000634582.1:c.13+3970A= ENSP00000489540.1:n.13+3970A=
ENST00000634640.1:c.-231+343A= ENSP00000489083.1:n.-231+343A=
ENST00000635045.1:n.485A=
ENST00000635543.1:c.400A= ENSP00000489205.1:p.Met134=
ENST00000635598.1:c.341+59A= ENSP00000489207.1:n.341+59A=
NM_002641.3:c.400A= , LRG_160t1:c.400A= NP_002632.1:p.Met134=
NM_020473.3:c.13+3970A= NP_065206.3:n.13+3970A=
NR_033835.1:n.457+59A=
NR_033836.1:n.173+343A=
NM_002641.4:c.400A= MANE Select NP_002632.1:p.Met134=