Canonical Allele Identifier: CA2640288192
Gene: GAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80110717dup , CM000679.2:g.80110717dup GRCh38
NC_000017.10:g.78084516dup , CM000679.1:g.78084516dup GRCh37
NC_000017.9:g.75699111dup NCBI36
NG_009822.1:g.14162dup , LRG_673:g.14162dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1438-10dup ENSP00000460543.2:n.1438-10dup
ENST00000572080.2:c.1438-10dup ENSP00000459972.2:n.1438-10dup
ENST00000577106.6:c.1438-10dup ENSP00000458306.2:n.1438-10dup
ENST00000302262.8:c.1438-10dup MANE Select ENSP00000305692.3:n.1438-10dup
ENST00000302262.7:c.1438-10dup ENSP00000305692.3:n.1438-10dup
ENST00000390015.7:c.1438-10dup ENSP00000374665.3:n.1438-10dup
NM_000152.3:c.1438-10dup , LRG_673t1:c.1438-10dup NP_000143.2:n.1438-10dup
NM_001079803.1:c.1438-10dup NP_001073271.1:n.1438-10dup
NM_001079804.1:c.1438-10dup NP_001073272.1:n.1438-10dup
XM_005257193.1:c.1438-10dup XP_005257250.1:n.1438-10dup
XM_005257194.3:c.1438-10dup XP_005257251.1:n.1438-10dup
NM_000152.4:c.1438-10dup NP_000143.2:n.1438-10dup
NM_001079803.2:c.1438-10dup NP_001073271.1:n.1438-10dup
NM_001079804.2:c.1438-10dup NP_001073272.1:n.1438-10dup
XM_005257193.2:c.1438-10dup XP_005257250.1:n.1438-10dup
XM_005257194.4:c.1438-10dup XP_005257251.1:n.1438-10dup
NM_000152.5:c.1438-10dup MANE Select NP_000143.2:n.1438-10dup
NM_001079803.3:c.1438-10dup NP_001073271.1:n.1438-10dup
NM_001079804.3:c.1438-10dup NP_001073272.1:n.1438-10dup