Canonical Allele Identifier: CA2277818216
Gene: GAA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118790_80118791delinsCA , CM000679.2:g.80118790_80118791delinsCA GRCh38
NC_000017.10:g.78092589_78092590delinsCA , CM000679.1:g.78092589_78092590delinsCA GRCh37
NC_000017.9:g.75707184_75707185delinsCA NCBI36
NG_009822.1:g.22235_22236delinsCA , LRG_673:g.22235_22236delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2784_2785delinsCA ENSP00000460543.2:p.Tyr928=
ENST00000572080.2:c.*922_*923delinsCA ENSP00000459972.2:n.*922_*923delinsCA
ENST00000577106.6:c.2784_2785delinsCA ENSP00000458306.2:p.Tyr928=
ENST00000302262.8:c.2784_2785delinsCA MANE Select ENSP00000305692.3:p.Tyr928=
ENST00000302262.7:c.2784_2785delinsCA ENSP00000305692.3:p.Tyr928=
ENST00000390015.7:c.2784_2785delinsCA ENSP00000374665.3:p.Tyr928=
ENST00000573556.1:n.737_738delinsCA
NM_000152.3:c.2784_2785delinsCA , LRG_673t1:c.2784_2785delinsCA NP_000143.2:p.Tyr928=
NM_001079803.1:c.2784_2785delinsCA NP_001073271.1:p.Tyr928=
NM_001079804.1:c.2784_2785delinsCA NP_001073272.1:p.Tyr928=
XM_005257193.1:c.2784_2785delinsCA XP_005257250.1:p.Tyr928=
XM_005257194.3:c.2784_2785delinsCA XP_005257251.1:p.Tyr928=
NM_000152.4:c.2784_2785delinsCA NP_000143.2:p.Tyr928=
NM_001079803.2:c.2784_2785delinsCA NP_001073271.1:p.Tyr928=
NM_001079804.2:c.2784_2785delinsCA NP_001073272.1:p.Tyr928=
XM_005257193.2:c.2784_2785delinsCA XP_005257250.1:p.Tyr928=
XM_005257194.4:c.2784_2785delinsCA XP_005257251.1:p.Tyr928=
NM_000152.5:c.2784_2785delinsCA MANE Select NP_000143.2:p.Tyr928=
NM_001079803.3:c.2784_2785delinsCA NP_001073271.1:p.Tyr928=
NM_001079804.3:c.2784_2785delinsCA NP_001073272.1:p.Tyr928=
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