Canonical Allele Identifier: CA401326319
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 943435
dbSNP Id: rs951742543

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118308A>C , CM000679.2:g.80118308A>C GRCh38
NC_000017.10:g.78092107A>C , CM000679.1:g.78092107A>C GRCh37
NC_000017.9:g.75706702A>C NCBI36
NG_009822.1:g.21753A>C , LRG_673:g.21753A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2597A>C ENSP00000460543.2:p.Glu866Ala
ENST00000572080.2:c.*735A>C ENSP00000459972.2:n.*735A>C
ENST00000577106.6:c.2597A>C ENSP00000458306.2:p.Glu866Ala
ENST00000302262.8:c.2597A>C MANE Select ENSP00000305692.3:p.Glu866Ala
ENST00000302262.7:c.2597A>C ENSP00000305692.3:p.Glu866Ala
ENST00000390015.7:c.2597A>C ENSP00000374665.3:p.Glu866Ala
ENST00000573556.1:n.550A>C
NM_000152.3:c.2597A>C , LRG_673t1:c.2597A>C NP_000143.2:p.Glu866Ala
NM_001079803.1:c.2597A>C NP_001073271.1:p.Glu866Ala
NM_001079804.1:c.2597A>C NP_001073272.1:p.Glu866Ala
XM_005257193.1:c.2597A>C XP_005257250.1:p.Glu866Ala
XM_005257194.3:c.2597A>C XP_005257251.1:p.Glu866Ala
NM_000152.4:c.2597A>C NP_000143.2:p.Glu866Ala
NM_001079803.2:c.2597A>C NP_001073271.1:p.Glu866Ala
NM_001079804.2:c.2597A>C NP_001073272.1:p.Glu866Ala
XM_005257193.2:c.2597A>C XP_005257250.1:p.Glu866Ala
XM_005257194.4:c.2597A>C XP_005257251.1:p.Glu866Ala
NM_000152.5:c.2597A>C MANE Select NP_000143.2:p.Glu866Ala
NM_001079803.3:c.2597A>C NP_001073271.1:p.Glu866Ala
NM_001079804.3:c.2597A>C NP_001073272.1:p.Glu866Ala