Canonical Allele Identifier: CA2277812574
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108130_80108131delinsGT , CM000679.2:g.80108130_80108131delinsGT GRCh38
NC_000017.10:g.78081929_78081930delinsGT , CM000679.1:g.78081929_78081930delinsGT GRCh37
NC_000017.9:g.75696524_75696525delinsGT NCBI36
NG_009822.1:g.11575_11576delinsGT , LRG_673:g.11575_11576delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.956-160_956-159delinsGT ENSP00000460543.2:n.956-160_956-159delinsGT
ENST00000572080.2:c.956-160_956-159delinsGT ENSP00000459972.2:n.956-160_956-159delinsGT
ENST00000577106.6:c.956-160_956-159delinsGT ENSP00000458306.2:n.956-160_956-159delinsGT
ENST00000302262.8:c.956-160_956-159delinsGT MANE Select ENSP00000305692.3:n.956-160_956-159delinsGT
ENST00000302262.7:c.956-160_956-159delinsGT ENSP00000305692.3:n.956-160_956-159delinsGT
ENST00000390015.7:c.956-160_956-159delinsGT ENSP00000374665.3:n.956-160_956-159delinsGT
NM_000152.3:c.956-160_956-159delinsGT , LRG_673t1:c.956-160_956-159delinsGT NP_000143.2:n.956-160_956-159delinsGT
NM_001079803.1:c.956-160_956-159delinsGT NP_001073271.1:n.956-160_956-159delinsGT
NM_001079804.1:c.956-160_956-159delinsGT NP_001073272.1:n.956-160_956-159delinsGT
XM_005257193.1:c.956-160_956-159delinsGT XP_005257250.1:n.956-160_956-159delinsGT
XM_005257194.3:c.956-160_956-159delinsGT XP_005257251.1:n.956-160_956-159delinsGT
NM_000152.4:c.956-160_956-159delinsGT NP_000143.2:n.956-160_956-159delinsGT
NM_001079803.2:c.956-160_956-159delinsGT NP_001073271.1:n.956-160_956-159delinsGT
NM_001079804.2:c.956-160_956-159delinsGT NP_001073272.1:n.956-160_956-159delinsGT
XM_005257193.2:c.956-160_956-159delinsGT XP_005257250.1:n.956-160_956-159delinsGT
XM_005257194.4:c.956-160_956-159delinsGT XP_005257251.1:n.956-160_956-159delinsGT
NM_000152.5:c.956-160_956-159delinsGT MANE Select NP_000143.2:n.956-160_956-159delinsGT
NM_001079803.3:c.956-160_956-159delinsGT NP_001073271.1:n.956-160_956-159delinsGT
NM_001079804.3:c.956-160_956-159delinsGT NP_001073272.1:n.956-160_956-159delinsGT