Canonical Allele Identifier: CA2277813023
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108867_80108874delinsCGCCCGGT , CM000679.2:g.80108867_80108874delinsCGCCCGGT GRCh38
NC_000017.10:g.78082666_78082673delinsCGCCCGGT , CM000679.1:g.78082666_78082673delinsCGCCCGGT GRCh37
NC_000017.9:g.75697261_75697268delinsCGCCCGGT NCBI36
NG_009822.1:g.12312_12319delinsCGCCCGGT , LRG_673:g.12312_12319delinsCGCCCGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1326+39_1326+46delinsCGCCCGGT ENSP00000460543.2:n.1326+39_1326+46delinsCGCCCGGT
ENST00000572080.2:c.1326+39_1326+46delinsCGCCCGGT ENSP00000459972.2:n.1326+39_1326+46delinsCGCCCGGT
ENST00000577106.6:c.1326+39_1326+46delinsCGCCCGGT ENSP00000458306.2:n.1326+39_1326+46delinsCGCCCGGT
ENST00000302262.8:c.1326+39_1326+46delinsCGCCCGGT MANE Select ENSP00000305692.3:n.1326+39_1326+46delinsCGCCCGGT
ENST00000302262.7:c.1326+39_1326+46delinsCGCCCGGT ENSP00000305692.3:n.1326+39_1326+46delinsCGCCCGGT
ENST00000390015.7:c.1326+39_1326+46delinsCGCCCGGT ENSP00000374665.3:n.1326+39_1326+46delinsCGCCCGGT
NM_000152.3:c.1326+39_1326+46delinsCGCCCGGT , LRG_673t1:c.1326+39_1326+46delinsCGCCCGGT NP_000143.2:n.1326+39_1326+46delinsCGCCCGGT
NM_001079803.1:c.1326+39_1326+46delinsCGCCCGGT NP_001073271.1:n.1326+39_1326+46delinsCGCCCGGT
NM_001079804.1:c.1326+39_1326+46delinsCGCCCGGT NP_001073272.1:n.1326+39_1326+46delinsCGCCCGGT
XM_005257193.1:c.1326+39_1326+46delinsCGCCCGGT XP_005257250.1:n.1326+39_1326+46delinsCGCCCGGT
XM_005257194.3:c.1326+39_1326+46delinsCGCCCGGT XP_005257251.1:n.1326+39_1326+46delinsCGCCCGGT
NM_000152.4:c.1326+39_1326+46delinsCGCCCGGT NP_000143.2:n.1326+39_1326+46delinsCGCCCGGT
NM_001079803.2:c.1326+39_1326+46delinsCGCCCGGT NP_001073271.1:n.1326+39_1326+46delinsCGCCCGGT
NM_001079804.2:c.1326+39_1326+46delinsCGCCCGGT NP_001073272.1:n.1326+39_1326+46delinsCGCCCGGT
XM_005257193.2:c.1326+39_1326+46delinsCGCCCGGT XP_005257250.1:n.1326+39_1326+46delinsCGCCCGGT
XM_005257194.4:c.1326+39_1326+46delinsCGCCCGGT XP_005257251.1:n.1326+39_1326+46delinsCGCCCGGT
NM_000152.5:c.1326+39_1326+46delinsCGCCCGGT MANE Select NP_000143.2:n.1326+39_1326+46delinsCGCCCGGT
NM_001079803.3:c.1326+39_1326+46delinsCGCCCGGT NP_001073271.1:n.1326+39_1326+46delinsCGCCCGGT
NM_001079804.3:c.1326+39_1326+46delinsCGCCCGGT NP_001073272.1:n.1326+39_1326+46delinsCGCCCGGT