Canonical Allele Identifier: CA2277809018
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101624A= , CM000679.2:g.80101624A= GRCh38
NC_000017.10:g.78075423A= , CM000679.1:g.78075423A= GRCh37
NC_000017.9:g.75690018A= NCBI36
NG_009822.1:g.5069A= , LRG_673:g.5069A=
NG_029761.1:g.69993A=

Transcript Alleles

HGVS Amino-acid change
ENST00000570803.6:c.-34A= ENSP00000460543.2:n.-34A=
ENST00000572080.2:c.-114A= ENSP00000459972.2:n.-114A=
ENST00000577106.6:c.-149A= ENSP00000458306.2:n.-149A=
ENST00000302262.8:c.-299A= MANE Select ENSP00000305692.3:n.-299A=
ENST00000390015.7:c.-114A= ENSP00000374665.3:n.-114A=
ENST00000570803.5:c.-34A= ENSP00000460543.1:n.-34A=
ENST00000574376.1:n.28A=
ENST00000577106.5:c.-149A= ENSP00000458306.1:n.-149A=
NM_000152.3:c.-299A= , LRG_673t1:c.-299A= NP_000143.2:n.-299A=
NM_001079803.1:c.-114A= NP_001073271.1:n.-114A=
NM_001079804.1:c.-34A= NP_001073272.1:n.-34A=
XM_005257193.1:c.-209A= XP_005257250.1:n.-209A=
XM_005257194.3:c.-149A= XP_005257251.1:n.-149A=
NM_000152.4:c.-299A= NP_000143.2:n.-299A=
NM_001079803.2:c.-114A= NP_001073271.1:n.-114A=
NM_001079804.2:c.-34A= NP_001073272.1:n.-34A=
NR_134848.1:n.99A=
XM_005257194.4:c.-149A= XP_005257251.1:n.-149A=
NM_000152.5:c.-299A= MANE Select NP_000143.2:n.-299A=
NM_001079803.3:c.-114A= NP_001073271.1:n.-114A=
NM_001079804.3:c.-34A= NP_001073272.1:n.-34A=
NR_134848.2:n.44A=