Canonical Allele Identifier: CA294856192
Gene: GAA HGNC NCBI

Linked Data

dbSNP Id: rs772976283

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80116744_80116745del , CM000679.2:g.80116744_80116745del GRCh38
NC_000017.10:g.78090543_78090544del , CM000679.1:g.78090543_78090544del GRCh37
NC_000017.9:g.75705138_75705139del NCBI36
NG_009822.1:g.20189_20190del , LRG_673:g.20189_20190del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2190-224_2190-223del ENSP00000460543.2:n.2190-224_2190-223del
ENST00000572080.2:c.*328-224_*328-223del ENSP00000459972.2:n.*328-224_*328-223del
ENST00000577106.6:c.2190-224_2190-223del ENSP00000458306.2:n.2190-224_2190-223del
ENST00000302262.8:c.2190-224_2190-223del MANE Select ENSP00000305692.3:n.2190-224_2190-223del
ENST00000302262.7:c.2190-224_2190-223del ENSP00000305692.3:n.2190-224_2190-223del
ENST00000390015.7:c.2190-224_2190-223del ENSP00000374665.3:n.2190-224_2190-223del
ENST00000572080.1:c.609-224_609-223del
NM_000152.3:c.2190-224_2190-223del , LRG_673t1:c.2190-224_2190-223del NP_000143.2:n.2190-224_2190-223del
NM_001079803.1:c.2190-224_2190-223del NP_001073271.1:n.2190-224_2190-223del
NM_001079804.1:c.2190-224_2190-223del NP_001073272.1:n.2190-224_2190-223del
XM_005257193.1:c.2190-224_2190-223del XP_005257250.1:n.2190-224_2190-223del
XM_005257194.3:c.2190-224_2190-223del XP_005257251.1:n.2190-224_2190-223del
NM_000152.4:c.2190-224_2190-223del NP_000143.2:n.2190-224_2190-223del
NM_001079803.2:c.2190-224_2190-223del NP_001073271.1:n.2190-224_2190-223del
NM_001079804.2:c.2190-224_2190-223del NP_001073272.1:n.2190-224_2190-223del
XM_005257193.2:c.2190-224_2190-223del XP_005257250.1:n.2190-224_2190-223del
XM_005257194.4:c.2190-224_2190-223del XP_005257251.1:n.2190-224_2190-223del
NM_000152.5:c.2190-224_2190-223del MANE Select NP_000143.2:n.2190-224_2190-223del
NM_001079803.3:c.2190-224_2190-223del NP_001073271.1:n.2190-224_2190-223del
NM_001079804.3:c.2190-224_2190-223del NP_001073272.1:n.2190-224_2190-223del