Canonical Allele Identifier: CA274067
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 188874
dbSNP Id: rs770276275

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80110029_80110032del , CM000679.2:g.80110029_80110032del GRCh38
NC_000017.10:g.78083828_78083831del , CM000679.1:g.78083828_78083831del GRCh37
NC_000017.9:g.75698423_75698426del NCBI36
NG_009822.1:g.13474_13477del , LRG_673:g.13474_13477del

Transcript Alleles

HGVS Amino-acid change
ENST00000570803.6:c.1411_1414del ENSP00000460543.2:p.Glu471ProfsTer5
ENST00000572080.2:c.1411_1414del ENSP00000459972.2:p.Glu471ProfsTer5
ENST00000577106.6:c.1411_1414del ENSP00000458306.2:p.Glu471ProfsTer5
ENST00000302262.8:c.1411_1414del MANE Select ENSP00000305692.3:p.Glu471ProfsTer5
ENST00000302262.7:c.1411_1414del ENSP00000305692.3:p.Glu471ProfsTer5
ENST00000390015.7:c.1411_1414del ENSP00000374665.3:p.Glu471ProfsTer5
NM_000152.3:c.1411_1414del , LRG_673t1:c.1411_1414del NP_000143.2:p.Glu471ProfsTer5
NM_001079803.1:c.1411_1414del NP_001073271.1:p.Glu471ProfsTer5
NM_001079804.1:c.1411_1414del NP_001073272.1:p.Glu471ProfsTer5
XM_005257193.1:c.1411_1414del XP_005257250.1:p.Glu471ProfsTer5
XM_005257194.3:c.1411_1414del XP_005257251.1:p.Glu471ProfsTer5
NM_000152.4:c.1411_1414del NP_000143.2:p.Glu471ProfsTer5
NM_001079803.2:c.1411_1414del NP_001073271.1:p.Glu471ProfsTer5
NM_001079804.2:c.1411_1414del NP_001073272.1:p.Glu471ProfsTer5
XM_005257193.2:c.1411_1414del XP_005257250.1:p.Glu471ProfsTer5
XM_005257194.4:c.1411_1414del XP_005257251.1:p.Glu471ProfsTer5
NM_000152.5:c.1411_1414del MANE Select NP_000143.2:p.Glu471ProfsTer5
NM_001079803.3:c.1411_1414del NP_001073271.1:p.Glu471ProfsTer5
NM_001079804.3:c.1411_1414del NP_001073272.1:p.Glu471ProfsTer5