Canonical Allele Identifier: CA986706033
Gene: GAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108800_80108801insCCAT , CM000679.2:g.80108800_80108801insCCAT GRCh38
NC_000017.10:g.78082599_78082600insCCAT , CM000679.1:g.78082599_78082600insCCAT GRCh37
NC_000017.9:g.75697194_75697195insCCAT NCBI36
NG_009822.1:g.12245_12246insCCAT , LRG_673:g.12245_12246insCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1298_1299insCCAT ENSP00000460543.2:p.Gln433HisfsTer?
ENST00000572080.2:c.1298_1299insCCAT ENSP00000459972.2:p.Gln433HisfsTer?
ENST00000577106.6:c.1298_1299insCCAT ENSP00000458306.2:p.Gln433HisfsTer?
ENST00000302262.8:c.1298_1299insCCAT MANE Select ENSP00000305692.3:p.Gln433HisfsTer?
ENST00000302262.7:c.1298_1299insCCAT ENSP00000305692.3:p.Gln433HisfsTer?
ENST00000390015.7:c.1298_1299insCCAT ENSP00000374665.3:p.Gln433HisfsTer?
NM_000152.3:c.1298_1299insCCAT , LRG_673t1:c.1298_1299insCCAT NP_000143.2:p.Gln433HisfsTer?
NM_001079803.1:c.1298_1299insCCAT NP_001073271.1:p.Gln433HisfsTer?
NM_001079804.1:c.1298_1299insCCAT NP_001073272.1:p.Gln433HisfsTer?
XM_005257193.1:c.1298_1299insCCAT XP_005257250.1:p.Gln433HisfsTer?
XM_005257194.3:c.1298_1299insCCAT XP_005257251.1:p.Gln433HisfsTer?
NM_000152.4:c.1298_1299insCCAT NP_000143.2:p.Gln433HisfsTer?
NM_001079803.2:c.1298_1299insCCAT NP_001073271.1:p.Gln433HisfsTer?
NM_001079804.2:c.1298_1299insCCAT NP_001073272.1:p.Gln433HisfsTer?
XM_005257193.2:c.1298_1299insCCAT XP_005257250.1:p.Gln433HisfsTer?
XM_005257194.4:c.1298_1299insCCAT XP_005257251.1:p.Gln433HisfsTer?
NM_000152.5:c.1298_1299insCCAT MANE Select NP_000143.2:p.Gln433HisfsTer?
NM_001079803.3:c.1298_1299insCCAT NP_001073271.1:p.Gln433HisfsTer?
NM_001079804.3:c.1298_1299insCCAT NP_001073272.1:p.Gln433HisfsTer?