Canonical Allele Identifier: CA2734102449
Gene: GAA HGNC NCBI

Linked Data

dbSNP Id: rs2143858683

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108829_80108830insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC , CM000679.2:g.80108829_80108830insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC GRCh38
NC_000017.10:g.78082628_78082629insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC , CM000679.1:g.78082628_78082629insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC GRCh37
NC_000017.9:g.75697223_75697224insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NCBI36
NG_009822.1:g.12274_12275insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC , LRG_673:g.12274_12275insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC ENSP00000460543.2:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCC...
ENST00000572080.2:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC ENSP00000459972.2:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCC...
ENST00000577106.6:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC ENSP00000458306.2:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCC...
ENST00000302262.8:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC MANE Select ENSP00000305692.3:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCC...
ENST00000302262.7:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC ENSP00000305692.3:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCC...
ENST00000390015.7:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC ENSP00000374665.3:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCC...
NM_000152.3:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC , LRG_673t1:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_000143.2:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGG...
NM_001079803.1:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_001073271.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
NM_001079804.1:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_001073272.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
XM_005257193.1:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC XP_005257250.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
XM_005257194.3:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC XP_005257251.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
NM_000152.4:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_000143.2:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGG...
NM_001079803.2:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_001073271.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
NM_001079804.2:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_001073272.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
XM_005257193.2:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC XP_005257250.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
XM_005257194.4:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC XP_005257251.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
NM_000152.5:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC MANE Select NP_000143.2:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGG...
NM_001079803.3:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_001073271.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...
NM_001079804.3:c.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGCCGGGAGCTACAGGCCC NP_001073272.1:n.1326+1_1326+2insATCCTGCCATCAGCAGCTCGGGCCCTGC...