Canonical Allele Identifier: CA2277809010
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80101617T= , CM000679.2:g.80101617T= GRCh38
NC_000017.10:g.78075416T= , CM000679.1:g.78075416T= GRCh37
NC_000017.9:g.75690011T= NCBI36
NG_009822.1:g.5062T= , LRG_673:g.5062T=
NG_029761.1:g.69986T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.-41T= ENSP00000460543.2:n.-41T=
ENST00000572080.2:c.-121T= ENSP00000459972.2:n.-121T=
ENST00000577106.6:c.-156T= ENSP00000458306.2:n.-156T=
ENST00000302262.8:c.-306T= MANE Select ENSP00000305692.3:n.-306T=
ENST00000390015.7:c.-121T= ENSP00000374665.3:n.-121T=
ENST00000570803.5:c.-41T= ENSP00000460543.1:n.-41T=
ENST00000574376.1:n.21T=
ENST00000577106.5:c.-156T= ENSP00000458306.1:n.-156T=
NM_000152.3:c.-306T= , LRG_673t1:c.-306T= NP_000143.2:n.-306T=
NM_001079803.1:c.-121T= NP_001073271.1:n.-121T=
NM_001079804.1:c.-41T= NP_001073272.1:n.-41T=
XM_005257194.3:c.-156T= XP_005257251.1:n.-156T=
NM_000152.4:c.-306T= NP_000143.2:n.-306T=
NM_001079803.2:c.-121T= NP_001073271.1:n.-121T=
NM_001079804.2:c.-41T= NP_001073272.1:n.-41T=
NR_134848.1:n.92T=
XM_005257194.4:c.-156T= XP_005257251.1:n.-156T=
NM_000152.5:c.-306T= MANE Select NP_000143.2:n.-306T=
NM_001079803.3:c.-121T= NP_001073271.1:n.-121T=
NM_001079804.3:c.-41T= NP_001073272.1:n.-41T=
NR_134848.2:n.37T=