Canonical Allele Identifier: CA2277815903
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80113982T= , CM000679.2:g.80113982T= GRCh38
NC_000017.10:g.78087781T= , CM000679.1:g.78087781T= GRCh37
NC_000017.9:g.75702376T= NCBI36
NG_009822.1:g.17427T= , LRG_673:g.17427T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2189+616T= ENSP00000460543.2:n.2189+616T=
ENST00000572080.2:c.*327+616T= ENSP00000459972.2:n.*327+616T=
ENST00000577106.6:c.2189+616T= ENSP00000458306.2:n.2189+616T=
ENST00000302262.8:c.2189+616T= MANE Select ENSP00000305692.3:n.2189+616T=
ENST00000302262.7:c.2189+616T= ENSP00000305692.3:n.2189+616T=
ENST00000390015.7:c.2189+616T= ENSP00000374665.3:n.2189+616T=
ENST00000572080.1:c.608+616T=
NM_000152.3:c.2189+616T= , LRG_673t1:c.2189+616T= NP_000143.2:n.2189+616T=
NM_001079803.1:c.2189+616T= NP_001073271.1:n.2189+616T=
NM_001079804.1:c.2189+616T= NP_001073272.1:n.2189+616T=
XM_005257193.1:c.2189+616T= XP_005257250.1:n.2189+616T=
XM_005257194.3:c.2189+616T= XP_005257251.1:n.2189+616T=
NM_000152.4:c.2189+616T= NP_000143.2:n.2189+616T=
NM_001079803.2:c.2189+616T= NP_001073271.1:n.2189+616T=
NM_001079804.2:c.2189+616T= NP_001073272.1:n.2189+616T=
XM_005257193.2:c.2189+616T= XP_005257250.1:n.2189+616T=
XM_005257194.4:c.2189+616T= XP_005257251.1:n.2189+616T=
NM_000152.5:c.2189+616T= MANE Select NP_000143.2:n.2189+616T=
NM_001079803.3:c.2189+616T= NP_001073271.1:n.2189+616T=
NM_001079804.3:c.2189+616T= NP_001073272.1:n.2189+616T=