Canonical Allele Identifier: CA8815140
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 291212
dbSNP Id: rs751918816

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108418T>C , CM000679.2:g.80108418T>C GRCh38
NC_000017.10:g.78082217T>C , CM000679.1:g.78082217T>C GRCh37
NC_000017.9:g.75696812T>C NCBI36
NG_009822.1:g.11863T>C , LRG_673:g.11863T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1075+9T>C ENSP00000460543.2:n.1075+9T>C
ENST00000572080.2:c.1075+9T>C ENSP00000459972.2:n.1075+9T>C
ENST00000577106.6:c.1075+9T>C ENSP00000458306.2:n.1075+9T>C
ENST00000302262.8:c.1075+9T>C MANE Select ENSP00000305692.3:n.1075+9T>C
ENST00000302262.7:c.1075+9T>C ENSP00000305692.3:n.1075+9T>C
ENST00000390015.7:c.1075+9T>C ENSP00000374665.3:n.1075+9T>C
NM_000152.3:c.1075+9T>C , LRG_673t1:c.1075+9T>C NP_000143.2:n.1075+9T>C
NM_001079803.1:c.1075+9T>C NP_001073271.1:n.1075+9T>C
NM_001079804.1:c.1075+9T>C NP_001073272.1:n.1075+9T>C
XM_005257193.1:c.1075+9T>C XP_005257250.1:n.1075+9T>C
XM_005257194.3:c.1075+9T>C XP_005257251.1:n.1075+9T>C
NM_000152.4:c.1075+9T>C NP_000143.2:n.1075+9T>C
NM_001079803.2:c.1075+9T>C NP_001073271.1:n.1075+9T>C
NM_001079804.2:c.1075+9T>C NP_001073272.1:n.1075+9T>C
XM_005257193.2:c.1075+9T>C XP_005257250.1:n.1075+9T>C
XM_005257194.4:c.1075+9T>C XP_005257251.1:n.1075+9T>C
NM_000152.5:c.1075+9T>C MANE Select NP_000143.2:n.1075+9T>C
NM_001079803.3:c.1075+9T>C NP_001073271.1:n.1075+9T>C
NM_001079804.3:c.1075+9T>C NP_001073272.1:n.1075+9T>C