Canonical Allele Identifier: CA2277814038
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80110708_80110723delinsGCAGCCTCTCGTTGTC , CM000679.2:g.80110708_80110723delinsGCAGCCTCTCGTTGTC GRCh38
NC_000017.10:g.78084507_78084522delinsGCAGCCTCTCGTTGTC , CM000679.1:g.78084507_78084522delinsGCAGCCTCTCGTTGTC GRCh37
NC_000017.9:g.75699102_75699117delinsGCAGCCTCTCGTTGTC NCBI36
NG_009822.1:g.14153_14168delinsGCAGCCTCTCGTTGTC , LRG_673:g.14153_14168delinsGCAGCCTCTCGTTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC ENSP00000460543.2:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
ENST00000572080.2:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC ENSP00000459972.2:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
ENST00000577106.6:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC ENSP00000458306.2:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
ENST00000302262.8:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC MANE Select ENSP00000305692.3:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
ENST00000302262.7:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC ENSP00000305692.3:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
ENST00000390015.7:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC ENSP00000374665.3:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_000152.3:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC , LRG_673t1:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_000143.2:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_001079803.1:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_001073271.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_001079804.1:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_001073272.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
XM_005257193.1:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC XP_005257250.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
XM_005257194.3:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC XP_005257251.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_000152.4:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_000143.2:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_001079803.2:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_001073271.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_001079804.2:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_001073272.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
XM_005257193.2:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC XP_005257250.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
XM_005257194.4:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC XP_005257251.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_000152.5:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC MANE Select NP_000143.2:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_001079803.3:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_001073271.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC
NM_001079804.3:c.1438-19_1438-4delinsGCAGCCTCTCGTTGTC NP_001073272.1:n.1438-19_1438-4delinsGCAGCCTCTCGTTGTC