Canonical Allele Identifier: CA2277817990
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118364_80118370delinsCCTGGGG , CM000679.2:g.80118364_80118370delinsCCTGGGG GRCh38
NC_000017.10:g.78092163_78092169delinsCCTGGGG , CM000679.1:g.78092163_78092169delinsCCTGGGG GRCh37
NC_000017.9:g.75706758_75706764delinsCCTGGGG NCBI36
NG_009822.1:g.21809_21815delinsCCTGGGG , LRG_673:g.21809_21815delinsCCTGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2646+7_2646+13delinsCCTGGGG ENSP00000460543.2:n.2646+7_2646+13delinsCCTGGGG
ENST00000572080.2:c.*784+7_*784+13delinsCCTGGGG ENSP00000459972.2:n.*784+7_*784+13delinsCCTGGGG
ENST00000577106.6:c.2646+7_2646+13delinsCCTGGGG ENSP00000458306.2:n.2646+7_2646+13delinsCCTGGGG
ENST00000302262.8:c.2646+7_2646+13delinsCCTGGGG MANE Select ENSP00000305692.3:n.2646+7_2646+13delinsCCTGGGG
ENST00000302262.7:c.2646+7_2646+13delinsCCTGGGG ENSP00000305692.3:n.2646+7_2646+13delinsCCTGGGG
ENST00000390015.7:c.2646+7_2646+13delinsCCTGGGG ENSP00000374665.3:n.2646+7_2646+13delinsCCTGGGG
ENST00000573556.1:n.599+7_599+13delinsCCTGGGG
NM_000152.3:c.2646+7_2646+13delinsCCTGGGG , LRG_673t1:c.2646+7_2646+13delinsCCTGGGG NP_000143.2:n.2646+7_2646+13delinsCCTGGGG
NM_001079803.1:c.2646+7_2646+13delinsCCTGGGG NP_001073271.1:n.2646+7_2646+13delinsCCTGGGG
NM_001079804.1:c.2646+7_2646+13delinsCCTGGGG NP_001073272.1:n.2646+7_2646+13delinsCCTGGGG
XM_005257193.1:c.2646+7_2646+13delinsCCTGGGG XP_005257250.1:n.2646+7_2646+13delinsCCTGGGG
XM_005257194.3:c.2646+7_2646+13delinsCCTGGGG XP_005257251.1:n.2646+7_2646+13delinsCCTGGGG
NM_000152.4:c.2646+7_2646+13delinsCCTGGGG NP_000143.2:n.2646+7_2646+13delinsCCTGGGG
NM_001079803.2:c.2646+7_2646+13delinsCCTGGGG NP_001073271.1:n.2646+7_2646+13delinsCCTGGGG
NM_001079804.2:c.2646+7_2646+13delinsCCTGGGG NP_001073272.1:n.2646+7_2646+13delinsCCTGGGG
XM_005257193.2:c.2646+7_2646+13delinsCCTGGGG XP_005257250.1:n.2646+7_2646+13delinsCCTGGGG
XM_005257194.4:c.2646+7_2646+13delinsCCTGGGG XP_005257251.1:n.2646+7_2646+13delinsCCTGGGG
NM_000152.5:c.2646+7_2646+13delinsCCTGGGG MANE Select NP_000143.2:n.2646+7_2646+13delinsCCTGGGG
NM_001079803.3:c.2646+7_2646+13delinsCCTGGGG NP_001073271.1:n.2646+7_2646+13delinsCCTGGGG
NM_001079804.3:c.2646+7_2646+13delinsCCTGGGG NP_001073272.1:n.2646+7_2646+13delinsCCTGGGG