Canonical Allele Identifier: CA2277815417
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80113234_80113235delinsGC , CM000679.2:g.80113234_80113235delinsGC GRCh38
NC_000017.10:g.78087033_78087034delinsGC , CM000679.1:g.78087033_78087034delinsGC GRCh37
NC_000017.9:g.75701628_75701629delinsGC NCBI36
NG_009822.1:g.16679_16680delinsGC , LRG_673:g.16679_16680delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2057_2058delinsGC ENSP00000460543.2:p.Ser686=
ENST00000572080.2:c.*195_*196delinsGC ENSP00000459972.2:n.*195_*196delinsGC
ENST00000577106.6:c.2057_2058delinsGC ENSP00000458306.2:p.Ser686=
ENST00000302262.8:c.2057_2058delinsGC MANE Select ENSP00000305692.3:p.Ser686=
ENST00000302262.7:c.2057_2058delinsGC ENSP00000305692.3:p.Ser686=
ENST00000390015.7:c.2057_2058delinsGC ENSP00000374665.3:p.Ser686=
ENST00000570716.1:n.497_498delinsGC
ENST00000572080.1:c.476_477delinsGC
NM_000152.3:c.2057_2058delinsGC , LRG_673t1:c.2057_2058delinsGC NP_000143.2:p.Ser686=
NM_001079803.1:c.2057_2058delinsGC NP_001073271.1:p.Ser686=
NM_001079804.1:c.2057_2058delinsGC NP_001073272.1:p.Ser686=
XM_005257193.1:c.2057_2058delinsGC XP_005257250.1:p.Ser686=
XM_005257194.3:c.2057_2058delinsGC XP_005257251.1:p.Ser686=
NM_000152.4:c.2057_2058delinsGC NP_000143.2:p.Ser686=
NM_001079803.2:c.2057_2058delinsGC NP_001073271.1:p.Ser686=
NM_001079804.2:c.2057_2058delinsGC NP_001073272.1:p.Ser686=
XM_005257193.2:c.2057_2058delinsGC XP_005257250.1:p.Ser686=
XM_005257194.4:c.2057_2058delinsGC XP_005257251.1:p.Ser686=
NM_000152.5:c.2057_2058delinsGC MANE Select NP_000143.2:p.Ser686=
NM_001079803.3:c.2057_2058delinsGC NP_001073271.1:p.Ser686=
NM_001079804.3:c.2057_2058delinsGC NP_001073272.1:p.Ser686=