Canonical Allele Identifier: CA2277812564
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108112_80108114delinsCTT , CM000679.2:g.80108112_80108114delinsCTT GRCh38
NC_000017.10:g.78081911_78081913delinsCTT , CM000679.1:g.78081911_78081913delinsCTT GRCh37
NC_000017.9:g.75696506_75696508delinsCTT NCBI36
NG_009822.1:g.11557_11559delinsCTT , LRG_673:g.11557_11559delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.956-178_956-176delinsCTT ENSP00000460543.2:n.956-178_956-176delinsCTT
ENST00000572080.2:c.956-178_956-176delinsCTT ENSP00000459972.2:n.956-178_956-176delinsCTT
ENST00000577106.6:c.956-178_956-176delinsCTT ENSP00000458306.2:n.956-178_956-176delinsCTT
ENST00000302262.8:c.956-178_956-176delinsCTT MANE Select ENSP00000305692.3:n.956-178_956-176delinsCTT
ENST00000302262.7:c.956-178_956-176delinsCTT ENSP00000305692.3:n.956-178_956-176delinsCTT
ENST00000390015.7:c.956-178_956-176delinsCTT ENSP00000374665.3:n.956-178_956-176delinsCTT
NM_000152.3:c.956-178_956-176delinsCTT , LRG_673t1:c.956-178_956-176delinsCTT NP_000143.2:n.956-178_956-176delinsCTT
NM_001079803.1:c.956-178_956-176delinsCTT NP_001073271.1:n.956-178_956-176delinsCTT
NM_001079804.1:c.956-178_956-176delinsCTT NP_001073272.1:n.956-178_956-176delinsCTT
XM_005257193.1:c.956-178_956-176delinsCTT XP_005257250.1:n.956-178_956-176delinsCTT
XM_005257194.3:c.956-178_956-176delinsCTT XP_005257251.1:n.956-178_956-176delinsCTT
NM_000152.4:c.956-178_956-176delinsCTT NP_000143.2:n.956-178_956-176delinsCTT
NM_001079803.2:c.956-178_956-176delinsCTT NP_001073271.1:n.956-178_956-176delinsCTT
NM_001079804.2:c.956-178_956-176delinsCTT NP_001073272.1:n.956-178_956-176delinsCTT
XM_005257193.2:c.956-178_956-176delinsCTT XP_005257250.1:n.956-178_956-176delinsCTT
XM_005257194.4:c.956-178_956-176delinsCTT XP_005257251.1:n.956-178_956-176delinsCTT
NM_000152.5:c.956-178_956-176delinsCTT MANE Select NP_000143.2:n.956-178_956-176delinsCTT
NM_001079803.3:c.956-178_956-176delinsCTT NP_001073271.1:n.956-178_956-176delinsCTT
NM_001079804.3:c.956-178_956-176delinsCTT NP_001073272.1:n.956-178_956-176delinsCTT