Canonical Allele Identifier: CA658795235
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 932903
ClinVar RCV Id: RCV001200871
dbSNP Id: rs2039116471

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80107586_80107587del , CM000679.2:g.80107586_80107587del GRCh38
NC_000017.10:g.78081385_78081386del , CM000679.1:g.78081385_78081386del GRCh37
NC_000017.9:g.75695980_75695981del NCBI36
NG_009822.1:g.11031_11032del , LRG_673:g.11031_11032del

Transcript Alleles

HGVS Amino-acid change
ENST00000570803.6:c.722_723del ENSP00000460543.2:p.Phe241CysfsTer?
ENST00000572080.2:c.722_723del ENSP00000459972.2:p.Phe241CysfsTer?
ENST00000577106.6:c.722_723del ENSP00000458306.2:p.Phe241CysfsTer?
ENST00000302262.8:c.722_723del MANE Select ENSP00000305692.3:p.Phe241CysfsTer?
ENST00000302262.7:c.722_723del ENSP00000305692.3:p.Phe241CysfsTer?
ENST00000390015.7:c.722_723del ENSP00000374665.3:p.Phe241CysfsTer?
ENST00000570803.5:c.722_723del ENSP00000460543.1:p.Phe241CysfsTer?
NM_000152.3:c.722_723del , LRG_673t1:c.722_723del NP_000143.2:p.Phe241CysfsTer?
NM_001079803.1:c.722_723del NP_001073271.1:p.Phe241CysfsTer?
NM_001079804.1:c.722_723del NP_001073272.1:p.Phe241CysfsTer?
XM_005257193.1:c.722_723del XP_005257250.1:p.Phe241CysfsTer?
XM_005257194.3:c.722_723del XP_005257251.1:p.Phe241CysfsTer?
NM_000152.4:c.722_723del NP_000143.2:p.Phe241CysfsTer?
NM_001079803.2:c.722_723del NP_001073271.1:p.Phe241CysfsTer?
NM_001079804.2:c.722_723del NP_001073272.1:p.Phe241CysfsTer?
XM_005257193.2:c.722_723del XP_005257250.1:p.Phe241CysfsTer?
XM_005257194.4:c.722_723del XP_005257251.1:p.Phe241CysfsTer?
NM_000152.5:c.722_723del MANE Select NP_000143.2:p.Phe241CysfsTer?
NM_001079803.3:c.722_723del NP_001073271.1:p.Phe241CysfsTer?
NM_001079804.3:c.722_723del NP_001073272.1:p.Phe241CysfsTer?