Canonical Allele Identifier: CA2277809014
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101621C= , CM000679.2:g.80101621C= GRCh38
NC_000017.10:g.78075420C= , CM000679.1:g.78075420C= GRCh37
NC_000017.9:g.75690015C= NCBI36
NG_009822.1:g.5066C= , LRG_673:g.5066C=
NG_029761.1:g.69990C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.-37C= ENSP00000460543.2:n.-37C=
ENST00000572080.2:c.-117C= ENSP00000459972.2:n.-117C=
ENST00000577106.6:c.-152C= ENSP00000458306.2:n.-152C=
ENST00000302262.8:c.-302C= MANE Select ENSP00000305692.3:n.-302C=
ENST00000390015.7:c.-117C= ENSP00000374665.3:n.-117C=
ENST00000570803.5:c.-37C= ENSP00000460543.1:n.-37C=
ENST00000574376.1:n.25C=
ENST00000577106.5:c.-152C= ENSP00000458306.1:n.-152C=
NM_000152.3:c.-302C= , LRG_673t1:c.-302C= NP_000143.2:n.-302C=
NM_001079803.1:c.-117C= NP_001073271.1:n.-117C=
NM_001079804.1:c.-37C= NP_001073272.1:n.-37C=
XM_005257193.1:c.-212C= XP_005257250.1:n.-212C=
XM_005257194.3:c.-152C= XP_005257251.1:n.-152C=
NM_000152.4:c.-302C= NP_000143.2:n.-302C=
NM_001079803.2:c.-117C= NP_001073271.1:n.-117C=
NM_001079804.2:c.-37C= NP_001073272.1:n.-37C=
NR_134848.1:n.96C=
XM_005257194.4:c.-152C= XP_005257251.1:n.-152C=
NM_000152.5:c.-302C= MANE Select NP_000143.2:n.-302C=
NM_001079803.3:c.-117C= NP_001073271.1:n.-117C=
NM_001079804.3:c.-37C= NP_001073272.1:n.-37C=
NR_134848.2:n.41C=