Canonical Allele Identifier: CA401367208
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 449460
dbSNP Id: rs892129065

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80110953C>A , CM000679.2:g.80110953C>A GRCh38
NC_000017.10:g.78084752C>A , CM000679.1:g.78084752C>A GRCh37
NC_000017.9:g.75699347C>A NCBI36
NG_009822.1:g.14398C>A , LRG_673:g.14398C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1564C>A ENSP00000460543.2:p.Pro522Thr
ENST00000572080.2:c.1564C>A ENSP00000459972.2:p.Pro522Thr
ENST00000577106.6:c.1564C>A ENSP00000458306.2:p.Pro522Thr
ENST00000302262.8:c.1564C>A MANE Select ENSP00000305692.3:p.Pro522Thr
ENST00000302262.7:c.1564C>A ENSP00000305692.3:p.Pro522Thr
ENST00000390015.7:c.1564C>A ENSP00000374665.3:p.Pro522Thr
NM_000152.3:c.1564C>A , LRG_673t1:c.1564C>A NP_000143.2:p.Pro522Thr
NM_001079803.1:c.1564C>A NP_001073271.1:p.Pro522Thr
NM_001079804.1:c.1564C>A NP_001073272.1:p.Pro522Thr
XM_005257193.1:c.1564C>A XP_005257250.1:p.Pro522Thr
XM_005257194.3:c.1564C>A XP_005257251.1:p.Pro522Thr
NM_000152.4:c.1564C>A NP_000143.2:p.Pro522Thr
NM_001079803.2:c.1564C>A NP_001073271.1:p.Pro522Thr
NM_001079804.2:c.1564C>A NP_001073272.1:p.Pro522Thr
XM_005257193.2:c.1564C>A XP_005257250.1:p.Pro522Thr
XM_005257194.4:c.1564C>A XP_005257251.1:p.Pro522Thr
NM_000152.5:c.1564C>A MANE Select NP_000143.2:p.Pro522Thr
NM_001079803.3:c.1564C>A NP_001073271.1:p.Pro522Thr
NM_001079804.3:c.1564C>A NP_001073272.1:p.Pro522Thr