Canonical Allele Identifier: CA2640287099
Gene: GAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80117231_80117232insACATGGCCGGGACT , CM000679.2:g.80117231_80117232insACATGGCCGGGACT GRCh38
NC_000017.10:g.78091030_78091031insACATGGCCGGGACT , CM000679.1:g.78091030_78091031insACATGGCCGGGACT GRCh37
NC_000017.9:g.75705625_75705626insACATGGCCGGGACT NCBI36
NG_009822.1:g.20676_20677insACATGGCCGGGACT , LRG_673:g.20676_20677insACATGGCCGGGACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2331+122_2331+123insACATGGCCGGGACT ENSP00000460543.2:n.2331+122_2331+123insACATGGCCGGGACT
ENST00000572080.2:c.*469+122_*469+123insACATGGCCGGGACT ENSP00000459972.2:n.*469+122_*469+123insACATGGCCGGGACT
ENST00000577106.6:c.2331+122_2331+123insACATGGCCGGGACT ENSP00000458306.2:n.2331+122_2331+123insACATGGCCGGGACT
ENST00000302262.8:c.2331+122_2331+123insACATGGCCGGGACT MANE Select ENSP00000305692.3:n.2331+122_2331+123insACATGGCCGGGACT
ENST00000302262.7:c.2331+122_2331+123insACATGGCCGGGACT ENSP00000305692.3:n.2331+122_2331+123insACATGGCCGGGACT
ENST00000390015.7:c.2331+122_2331+123insACATGGCCGGGACT ENSP00000374665.3:n.2331+122_2331+123insACATGGCCGGGACT
ENST00000573556.1:n.284+122_284+123insACATGGCCGGGACT
NM_000152.3:c.2331+122_2331+123insACATGGCCGGGACT , LRG_673t1:c.2331+122_2331+123insACATGGCCGGGACT NP_000143.2:n.2331+122_2331+123insACATGGCCGGGACT
NM_001079803.1:c.2331+122_2331+123insACATGGCCGGGACT NP_001073271.1:n.2331+122_2331+123insACATGGCCGGGACT
NM_001079804.1:c.2331+122_2331+123insACATGGCCGGGACT NP_001073272.1:n.2331+122_2331+123insACATGGCCGGGACT
XM_005257193.1:c.2331+122_2331+123insACATGGCCGGGACT XP_005257250.1:n.2331+122_2331+123insACATGGCCGGGACT
XM_005257194.3:c.2331+122_2331+123insACATGGCCGGGACT XP_005257251.1:n.2331+122_2331+123insACATGGCCGGGACT
NM_000152.4:c.2331+122_2331+123insACATGGCCGGGACT NP_000143.2:n.2331+122_2331+123insACATGGCCGGGACT
NM_001079803.2:c.2331+122_2331+123insACATGGCCGGGACT NP_001073271.1:n.2331+122_2331+123insACATGGCCGGGACT
NM_001079804.2:c.2331+122_2331+123insACATGGCCGGGACT NP_001073272.1:n.2331+122_2331+123insACATGGCCGGGACT
XM_005257193.2:c.2331+122_2331+123insACATGGCCGGGACT XP_005257250.1:n.2331+122_2331+123insACATGGCCGGGACT
XM_005257194.4:c.2331+122_2331+123insACATGGCCGGGACT XP_005257251.1:n.2331+122_2331+123insACATGGCCGGGACT
NM_000152.5:c.2331+122_2331+123insACATGGCCGGGACT MANE Select NP_000143.2:n.2331+122_2331+123insACATGGCCGGGACT
NM_001079803.3:c.2331+122_2331+123insACATGGCCGGGACT NP_001073271.1:n.2331+122_2331+123insACATGGCCGGGACT
NM_001079804.3:c.2331+122_2331+123insACATGGCCGGGACT NP_001073272.1:n.2331+122_2331+123insACATGGCCGGGACT