Canonical Allele Identifier: CA2965194681
Gene: GAA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105795dup , CM000679.2:g.80105795dup GRCh38
NC_000017.10:g.78079594dup , CM000679.1:g.78079594dup GRCh37
NC_000017.9:g.75694189dup NCBI36
NG_009822.1:g.9240dup , LRG_673:g.9240dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.593dup ENSP00000460543.2:p.His199AlafsTer?
ENST00000572080.2:c.593dup ENSP00000459972.2:p.His199AlafsTer?
ENST00000577106.6:c.593dup ENSP00000458306.2:p.His199AlafsTer?
ENST00000302262.8:c.593dup MANE Select ENSP00000305692.3:p.His199AlafsTer?
ENST00000302262.7:c.593dup ENSP00000305692.3:p.His199AlafsTer?
ENST00000390015.7:c.593dup ENSP00000374665.3:p.His199AlafsTer?
ENST00000570803.5:c.593dup ENSP00000460543.1:p.His199AlafsTer?
ENST00000577106.5:c.593dup ENSP00000458306.1:p.His199AlafsTer?
NM_000152.3:c.593dup , LRG_673t1:c.593dup NP_000143.2:p.His199AlafsTer?
NM_001079803.1:c.593dup NP_001073271.1:p.His199AlafsTer?
NM_001079804.1:c.593dup NP_001073272.1:p.His199AlafsTer?
XM_005257193.1:c.593dup XP_005257250.1:p.His199AlafsTer?
XM_005257194.3:c.593dup XP_005257251.1:p.His199AlafsTer?
NM_000152.4:c.593dup NP_000143.2:p.His199AlafsTer?
NM_001079803.2:c.593dup NP_001073271.1:p.His199AlafsTer?
NM_001079804.2:c.593dup NP_001073272.1:p.His199AlafsTer?
XM_005257193.2:c.593dup XP_005257250.1:p.His199AlafsTer?
XM_005257194.4:c.593dup XP_005257251.1:p.His199AlafsTer?
NM_000152.5:c.593dup MANE Select NP_000143.2:p.His199AlafsTer?
NM_001079803.3:c.593dup NP_001073271.1:p.His199AlafsTer?
NM_001079804.3:c.593dup NP_001073272.1:p.His199AlafsTer?
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