Canonical Allele Identifier: CA16607903
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 392862
dbSNP Id: rs1057524664

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80117094G>T , CM000679.2:g.80117094G>T GRCh38
NC_000017.10:g.78090893G>T , CM000679.1:g.78090893G>T GRCh37
NC_000017.9:g.75705488G>T NCBI36
NG_009822.1:g.20539G>T , LRG_673:g.20539G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2316G>T ENSP00000460543.2:p.Trp772Cys
ENST00000572080.2:c.*454G>T ENSP00000459972.2:n.*454G>T
ENST00000577106.6:c.2316G>T ENSP00000458306.2:p.Trp772Cys
ENST00000302262.8:c.2316G>T MANE Select ENSP00000305692.3:p.Trp772Cys
ENST00000302262.7:c.2316G>T ENSP00000305692.3:p.Trp772Cys
ENST00000390015.7:c.2316G>T ENSP00000374665.3:p.Trp772Cys
ENST00000573556.1:n.269G>T
NM_000152.3:c.2316G>T , LRG_673t1:c.2316G>T NP_000143.2:p.Trp772Cys
NM_001079803.1:c.2316G>T NP_001073271.1:p.Trp772Cys
NM_001079804.1:c.2316G>T NP_001073272.1:p.Trp772Cys
XM_005257193.1:c.2316G>T XP_005257250.1:p.Trp772Cys
XM_005257194.3:c.2316G>T XP_005257251.1:p.Trp772Cys
NM_000152.4:c.2316G>T NP_000143.2:p.Trp772Cys
NM_001079803.2:c.2316G>T NP_001073271.1:p.Trp772Cys
NM_001079804.2:c.2316G>T NP_001073272.1:p.Trp772Cys
XM_005257193.2:c.2316G>T XP_005257250.1:p.Trp772Cys
XM_005257194.4:c.2316G>T XP_005257251.1:p.Trp772Cys
NM_000152.5:c.2316G>T MANE Select NP_000143.2:p.Trp772Cys
NM_001079803.3:c.2316G>T NP_001073271.1:p.Trp772Cys
NM_001079804.3:c.2316G>T NP_001073272.1:p.Trp772Cys