Canonical Allele Identifier: CA2640269653
Gene: GAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101649G>T , CM000679.2:g.80101649G>T GRCh38
NC_000017.10:g.78075448G>T , CM000679.1:g.78075448G>T GRCh37
NC_000017.9:g.75690043G>T NCBI36
NG_009822.1:g.5094G>T , LRG_673:g.5094G>T
NG_029761.1:g.70018G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000570803.6:c.-33+24G>T ENSP00000460543.2:n.-33+24G>T
ENST00000572080.2:c.-113+24G>T ENSP00000459972.2:n.-113+24G>T
ENST00000577106.6:c.-148+24G>T ENSP00000458306.2:n.-148+24G>T
ENST00000302262.8:c.-274G>T MANE Select ENSP00000305692.3:n.-274G>T
ENST00000390015.7:c.-113+24G>T ENSP00000374665.3:n.-113+24G>T
ENST00000570803.5:c.-33+24G>T ENSP00000460543.1:n.-33+24G>T
ENST00000574376.1:n.29+24G>T
ENST00000577106.5:c.-148+24G>T ENSP00000458306.1:n.-148+24G>T
NM_000152.3:c.-274G>T , LRG_673t1:c.-274G>T NP_000143.2:n.-274G>T
NM_001079803.1:c.-113+24G>T NP_001073271.1:n.-113+24G>T
NM_001079804.1:c.-33+24G>T NP_001073272.1:n.-33+24G>T
XM_005257193.1:c.-184G>T XP_005257250.1:n.-184G>T
XM_005257194.3:c.-148+24G>T XP_005257251.1:n.-148+24G>T
NM_000152.4:c.-274G>T NP_000143.2:n.-274G>T
NM_001079803.2:c.-113+24G>T NP_001073271.1:n.-113+24G>T
NM_001079804.2:c.-33+24G>T NP_001073272.1:n.-33+24G>T
NR_134848.1:n.100+24G>T
XM_005257193.2:c.-184G>T XP_005257250.1:n.-184G>T
XM_005257194.4:c.-148+24G>T XP_005257251.1:n.-148+24G>T
NM_000152.5:c.-274G>T MANE Select NP_000143.2:n.-274G>T
NM_001079803.3:c.-113+24G>T NP_001073271.1:n.-113+24G>T
NM_001079804.3:c.-33+24G>T NP_001073272.1:n.-33+24G>T
NR_134848.2:n.45+24G>T