Canonical Allele Identifier: CA2277815805
Gene: GAA HGNC NCBI

Linked Data

dbSNP Id: rs2039304208

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80113836_80113837insCCCGGCTAAAAC , CM000679.2:g.80113836_80113837insCCCGGCTAAAAC GRCh38
NC_000017.10:g.78087635_78087636insCCCGGCTAAAAC , CM000679.1:g.78087635_78087636insCCCGGCTAAAAC GRCh37
NC_000017.9:g.75702230_75702231insCCCGGCTAAAAC NCBI36
NG_009822.1:g.17281_17282insCCCGGCTAAAAC , LRG_673:g.17281_17282insCCCGGCTAAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2189+470_2189+471insCCCGGCTAAAAC ENSP00000460543.2:n.2189+470_2189+471insCCCGGCTAAAAC
ENST00000572080.2:c.*327+470_*327+471insCCCGGCTAAAAC ENSP00000459972.2:n.*327+470_*327+471insCCCGGCTAAAAC
ENST00000577106.6:c.2189+470_2189+471insCCCGGCTAAAAC ENSP00000458306.2:n.2189+470_2189+471insCCCGGCTAAAAC
ENST00000302262.8:c.2189+470_2189+471insCCCGGCTAAAAC MANE Select ENSP00000305692.3:n.2189+470_2189+471insCCCGGCTAAAAC
ENST00000302262.7:c.2189+470_2189+471insCCCGGCTAAAAC ENSP00000305692.3:n.2189+470_2189+471insCCCGGCTAAAAC
ENST00000390015.7:c.2189+470_2189+471insCCCGGCTAAAAC ENSP00000374665.3:n.2189+470_2189+471insCCCGGCTAAAAC
ENST00000572080.1:c.608+470_608+471insCCCGGCTAAAAC
NM_000152.3:c.2189+470_2189+471insCCCGGCTAAAAC , LRG_673t1:c.2189+470_2189+471insCCCGGCTAAAAC NP_000143.2:n.2189+470_2189+471insCCCGGCTAAAAC
NM_001079803.1:c.2189+470_2189+471insCCCGGCTAAAAC NP_001073271.1:n.2189+470_2189+471insCCCGGCTAAAAC
NM_001079804.1:c.2189+470_2189+471insCCCGGCTAAAAC NP_001073272.1:n.2189+470_2189+471insCCCGGCTAAAAC
XM_005257193.1:c.2189+470_2189+471insCCCGGCTAAAAC XP_005257250.1:n.2189+470_2189+471insCCCGGCTAAAAC
XM_005257194.3:c.2189+470_2189+471insCCCGGCTAAAAC XP_005257251.1:n.2189+470_2189+471insCCCGGCTAAAAC
NM_000152.4:c.2189+470_2189+471insCCCGGCTAAAAC NP_000143.2:n.2189+470_2189+471insCCCGGCTAAAAC
NM_001079803.2:c.2189+470_2189+471insCCCGGCTAAAAC NP_001073271.1:n.2189+470_2189+471insCCCGGCTAAAAC
NM_001079804.2:c.2189+470_2189+471insCCCGGCTAAAAC NP_001073272.1:n.2189+470_2189+471insCCCGGCTAAAAC
XM_005257193.2:c.2189+470_2189+471insCCCGGCTAAAAC XP_005257250.1:n.2189+470_2189+471insCCCGGCTAAAAC
XM_005257194.4:c.2189+470_2189+471insCCCGGCTAAAAC XP_005257251.1:n.2189+470_2189+471insCCCGGCTAAAAC
NM_000152.5:c.2189+470_2189+471insCCCGGCTAAAAC MANE Select NP_000143.2:n.2189+470_2189+471insCCCGGCTAAAAC
NM_001079803.3:c.2189+470_2189+471insCCCGGCTAAAAC NP_001073271.1:n.2189+470_2189+471insCCCGGCTAAAAC
NM_001079804.3:c.2189+470_2189+471insCCCGGCTAAAAC NP_001073272.1:n.2189+470_2189+471insCCCGGCTAAAAC