Canonical Allele Identifier: CA986719330
Gene: GAA HGNC NCBI

Linked Data

dbSNP Id: rs2038949679

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101614G>A , CM000679.2:g.80101614G>A GRCh38
NC_000017.10:g.78075413G>A , CM000679.1:g.78075413G>A GRCh37
NC_000017.9:g.75690008G>A NCBI36
NG_009822.1:g.5059G>A , LRG_673:g.5059G>A
NG_029761.1:g.69983G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.-44G>A ENSP00000460543.2:n.-44G>A
ENST00000572080.2:c.-124G>A ENSP00000459972.2:n.-124G>A
ENST00000577106.6:c.-159G>A ENSP00000458306.2:n.-159G>A
ENST00000302262.8:c.-309G>A MANE Select ENSP00000305692.3:n.-309G>A
ENST00000390015.7:c.-124G>A ENSP00000374665.3:n.-124G>A
ENST00000570803.5:c.-44G>A ENSP00000460543.1:n.-44G>A
ENST00000574376.1:n.18G>A
ENST00000577106.5:c.-159G>A ENSP00000458306.1:n.-159G>A
NM_000152.3:c.-309G>A , LRG_673t1:c.-309G>A NP_000143.2:n.-309G>A
NM_001079803.1:c.-124G>A NP_001073271.1:n.-124G>A
NM_001079804.1:c.-44G>A NP_001073272.1:n.-44G>A
XM_005257194.3:c.-159G>A XP_005257251.1:n.-159G>A
NM_000152.4:c.-309G>A NP_000143.2:n.-309G>A
NM_001079803.2:c.-124G>A NP_001073271.1:n.-124G>A
NM_001079804.2:c.-44G>A NP_001073272.1:n.-44G>A
NR_134848.1:n.89G>A
XM_005257194.4:c.-159G>A XP_005257251.1:n.-159G>A
NM_000152.5:c.-309G>A MANE Select NP_000143.2:n.-309G>A
NM_001079803.3:c.-124G>A NP_001073271.1:n.-124G>A
NM_001079804.3:c.-44G>A NP_001073272.1:n.-44G>A
NR_134848.2:n.34G>A