Canonical Allele Identifier: CA775519704
Gene: GAA HGNC NCBI

Linked Data

dbSNP Id: rs1379879472

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80113953_80113954del , CM000679.2:g.80113953_80113954del GRCh38
NC_000017.10:g.78087752_78087753del , CM000679.1:g.78087752_78087753del GRCh37
NC_000017.9:g.75702347_75702348del NCBI36
NG_009822.1:g.17398_17399del , LRG_673:g.17398_17399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2189+587_2189+588del ENSP00000460543.2:n.2189+587_2189+588del
ENST00000572080.2:c.*327+587_*327+588del ENSP00000459972.2:n.*327+587_*327+588del
ENST00000577106.6:c.2189+587_2189+588del ENSP00000458306.2:n.2189+587_2189+588del
ENST00000302262.8:c.2189+587_2189+588del MANE Select ENSP00000305692.3:n.2189+587_2189+588del
ENST00000302262.7:c.2189+587_2189+588del ENSP00000305692.3:n.2189+587_2189+588del
ENST00000390015.7:c.2189+587_2189+588del ENSP00000374665.3:n.2189+587_2189+588del
ENST00000572080.1:c.608+587_608+588del
NM_000152.3:c.2189+587_2189+588del , LRG_673t1:c.2189+587_2189+588del NP_000143.2:n.2189+587_2189+588del
NM_001079803.1:c.2189+587_2189+588del NP_001073271.1:n.2189+587_2189+588del
NM_001079804.1:c.2189+587_2189+588del NP_001073272.1:n.2189+587_2189+588del
XM_005257193.1:c.2189+587_2189+588del XP_005257250.1:n.2189+587_2189+588del
XM_005257194.3:c.2189+587_2189+588del XP_005257251.1:n.2189+587_2189+588del
NM_000152.4:c.2189+587_2189+588del NP_000143.2:n.2189+587_2189+588del
NM_001079803.2:c.2189+587_2189+588del NP_001073271.1:n.2189+587_2189+588del
NM_001079804.2:c.2189+587_2189+588del NP_001073272.1:n.2189+587_2189+588del
XM_005257193.2:c.2189+587_2189+588del XP_005257250.1:n.2189+587_2189+588del
XM_005257194.4:c.2189+587_2189+588del XP_005257251.1:n.2189+587_2189+588del
NM_000152.5:c.2189+587_2189+588del MANE Select NP_000143.2:n.2189+587_2189+588del
NM_001079803.3:c.2189+587_2189+588del NP_001073271.1:n.2189+587_2189+588del
NM_001079804.3:c.2189+587_2189+588del NP_001073272.1:n.2189+587_2189+588del