Canonical Allele Identifier: CA2640289506
Gene: GAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80111143_80111144insAT , CM000679.2:g.80111143_80111144insAT GRCh38
NC_000017.10:g.78084942_78084943insAT , CM000679.1:g.78084942_78084943insAT GRCh37
NC_000017.9:g.75699537_75699538insAT NCBI36
NG_009822.1:g.14588_14589insAT , LRG_673:g.14588_14589insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1636+118_1636+119insAT ENSP00000460543.2:n.1636+118_1636+119insAT
ENST00000572080.2:c.1636+118_1636+119insAT ENSP00000459972.2:n.1636+118_1636+119insAT
ENST00000577106.6:c.1636+118_1636+119insAT ENSP00000458306.2:n.1636+118_1636+119insAT
ENST00000302262.8:c.1636+118_1636+119insAT MANE Select ENSP00000305692.3:n.1636+118_1636+119insAT
ENST00000302262.7:c.1636+118_1636+119insAT ENSP00000305692.3:n.1636+118_1636+119insAT
ENST00000390015.7:c.1636+118_1636+119insAT ENSP00000374665.3:n.1636+118_1636+119insAT
ENST00000572080.1:c.24+118_24+119insAT
NM_000152.3:c.1636+118_1636+119insAT , LRG_673t1:c.1636+118_1636+119insAT NP_000143.2:n.1636+118_1636+119insAT
NM_001079803.1:c.1636+118_1636+119insAT NP_001073271.1:n.1636+118_1636+119insAT
NM_001079804.1:c.1636+118_1636+119insAT NP_001073272.1:n.1636+118_1636+119insAT
XM_005257193.1:c.1636+118_1636+119insAT XP_005257250.1:n.1636+118_1636+119insAT
XM_005257194.3:c.1636+118_1636+119insAT XP_005257251.1:n.1636+118_1636+119insAT
NM_000152.4:c.1636+118_1636+119insAT NP_000143.2:n.1636+118_1636+119insAT
NM_001079803.2:c.1636+118_1636+119insAT NP_001073271.1:n.1636+118_1636+119insAT
NM_001079804.2:c.1636+118_1636+119insAT NP_001073272.1:n.1636+118_1636+119insAT
XM_005257193.2:c.1636+118_1636+119insAT XP_005257250.1:n.1636+118_1636+119insAT
XM_005257194.4:c.1636+118_1636+119insAT XP_005257251.1:n.1636+118_1636+119insAT
NM_000152.5:c.1636+118_1636+119insAT MANE Select NP_000143.2:n.1636+118_1636+119insAT
NM_001079803.3:c.1636+118_1636+119insAT NP_001073271.1:n.1636+118_1636+119insAT
NM_001079804.3:c.1636+118_1636+119insAT NP_001073272.1:n.1636+118_1636+119insAT