Canonical Allele Identifier: CA2277809020
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101634G= , CM000679.2:g.80101634G= GRCh38
NC_000017.10:g.78075433G= , CM000679.1:g.78075433G= GRCh37
NC_000017.9:g.75690028G= NCBI36
NG_009822.1:g.5079G= , LRG_673:g.5079G=
NG_029761.1:g.70003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.-33+9G= ENSP00000460543.2:n.-33+9G=
ENST00000572080.2:c.-113+9G= ENSP00000459972.2:n.-113+9G=
ENST00000577106.6:c.-148+9G= ENSP00000458306.2:n.-148+9G=
ENST00000302262.8:c.-289G= MANE Select ENSP00000305692.3:n.-289G=
ENST00000390015.7:c.-113+9G= ENSP00000374665.3:n.-113+9G=
ENST00000570803.5:c.-33+9G= ENSP00000460543.1:n.-33+9G=
ENST00000574376.1:n.29+9G=
ENST00000577106.5:c.-148+9G= ENSP00000458306.1:n.-148+9G=
NM_000152.3:c.-289G= , LRG_673t1:c.-289G= NP_000143.2:n.-289G=
NM_001079803.1:c.-113+9G= NP_001073271.1:n.-113+9G=
NM_001079804.1:c.-33+9G= NP_001073272.1:n.-33+9G=
XM_005257193.1:c.-199G= XP_005257250.1:n.-199G=
XM_005257194.3:c.-148+9G= XP_005257251.1:n.-148+9G=
NM_000152.4:c.-289G= NP_000143.2:n.-289G=
NM_001079803.2:c.-113+9G= NP_001073271.1:n.-113+9G=
NM_001079804.2:c.-33+9G= NP_001073272.1:n.-33+9G=
NR_134848.1:n.100+9G=
XM_005257194.4:c.-148+9G= XP_005257251.1:n.-148+9G=
NM_000152.5:c.-289G= MANE Select NP_000143.2:n.-289G=
NM_001079803.3:c.-113+9G= NP_001073271.1:n.-113+9G=
NM_001079804.3:c.-33+9G= NP_001073272.1:n.-33+9G=
NR_134848.2:n.45+9G=