Canonical Allele Identifier: CA2277809019
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101631C= , CM000679.2:g.80101631C= GRCh38
NC_000017.10:g.78075430C= , CM000679.1:g.78075430C= GRCh37
NC_000017.9:g.75690025C= NCBI36
NG_009822.1:g.5076C= , LRG_673:g.5076C=
NG_029761.1:g.70000C=

Transcript Alleles

HGVS Amino-acid change
ENST00000570803.6:c.-33+6C= ENSP00000460543.2:n.-33+6C=
ENST00000572080.2:c.-113+6C= ENSP00000459972.2:n.-113+6C=
ENST00000577106.6:c.-148+6C= ENSP00000458306.2:n.-148+6C=
ENST00000302262.8:c.-292C= MANE Select ENSP00000305692.3:n.-292C=
ENST00000390015.7:c.-113+6C= ENSP00000374665.3:n.-113+6C=
ENST00000570803.5:c.-33+6C= ENSP00000460543.1:n.-33+6C=
ENST00000574376.1:n.29+6C=
ENST00000577106.5:c.-148+6C= ENSP00000458306.1:n.-148+6C=
NM_000152.3:c.-292C= , LRG_673t1:c.-292C= NP_000143.2:n.-292C=
NM_001079803.1:c.-113+6C= NP_001073271.1:n.-113+6C=
NM_001079804.1:c.-33+6C= NP_001073272.1:n.-33+6C=
XM_005257193.1:c.-202C= XP_005257250.1:n.-202C=
XM_005257194.3:c.-148+6C= XP_005257251.1:n.-148+6C=
NM_000152.4:c.-292C= NP_000143.2:n.-292C=
NM_001079803.2:c.-113+6C= NP_001073271.1:n.-113+6C=
NM_001079804.2:c.-33+6C= NP_001073272.1:n.-33+6C=
NR_134848.1:n.100+6C=
XM_005257194.4:c.-148+6C= XP_005257251.1:n.-148+6C=
NM_000152.5:c.-292C= MANE Select NP_000143.2:n.-292C=
NM_001079803.3:c.-113+6C= NP_001073271.1:n.-113+6C=
NM_001079804.3:c.-33+6C= NP_001073272.1:n.-33+6C=
NR_134848.2:n.45+6C=