Canonical Allele Identifier: CA2277814179
Gene: GAA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80110941G= , CM000679.2:g.80110941G= GRCh38
NC_000017.10:g.78084740G= , CM000679.1:g.78084740G= GRCh37
NC_000017.9:g.75699335G= NCBI36
NG_009822.1:g.14386G= , LRG_673:g.14386G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1552G= ENSP00000460543.2:p.Asp518=
ENST00000572080.2:c.1552G= ENSP00000459972.2:p.Asp518=
ENST00000577106.6:c.1552G= ENSP00000458306.2:p.Asp518=
ENST00000302262.8:c.1552G= MANE Select ENSP00000305692.3:p.Asp518=
ENST00000302262.7:c.1552G= ENSP00000305692.3:p.Asp518=
ENST00000390015.7:c.1552G= ENSP00000374665.3:p.Asp518=
NM_000152.3:c.1552G= , LRG_673t1:c.1552G= NP_000143.2:p.Asp518=
NM_001079803.1:c.1552G= NP_001073271.1:p.Asp518=
NM_001079804.1:c.1552G= NP_001073272.1:p.Asp518=
XM_005257193.1:c.1552G= XP_005257250.1:p.Asp518=
XM_005257194.3:c.1552G= XP_005257251.1:p.Asp518=
NM_000152.4:c.1552G= NP_000143.2:p.Asp518=
NM_001079803.2:c.1552G= NP_001073271.1:p.Asp518=
NM_001079804.2:c.1552G= NP_001073272.1:p.Asp518=
XM_005257193.2:c.1552G= XP_005257250.1:p.Asp518=
XM_005257194.4:c.1552G= XP_005257251.1:p.Asp518=
NM_000152.5:c.1552G= MANE Select NP_000143.2:p.Asp518=
NM_001079803.3:c.1552G= NP_001073271.1:p.Asp518=
NM_001079804.3:c.1552G= NP_001073272.1:p.Asp518=
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