Canonical Allele Identifier: CA401369918
Community Standard Title: NM_000152.5(GAA):c.1940G>A (p.Cys647Tyr)
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80112927G>A , CM000679.2:g.80112927G>A GRCh38
NC_000017.10:g.78086726G>A , CM000679.1:g.78086726G>A GRCh37
NC_000017.9:g.75701321G>A NCBI36
NG_009822.1:g.16372G>A , LRG_673:g.16372G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000152.5:c.1940G>A MANE Select NP_000143.2:p.Cys647Tyr
ENST00000302262.8:c.1940G>A MANE Select ENSP00000305692.3:p.Cys647Tyr
NM_000152.3:c.1940G>A , LRG_673t1:c.1940G>A NP_000143.2:p.Cys647Tyr
NM_000152.4:c.1940G>A NP_000143.2:p.Cys647Tyr
NM_001079803.1:c.1940G>A NP_001073271.1:p.Cys647Tyr
NM_001079803.2:c.1940G>A NP_001073271.1:p.Cys647Tyr
NM_001079803.3:c.1940G>A NP_001073271.1:p.Cys647Tyr
NM_001079804.1:c.1940G>A NP_001073272.1:p.Cys647Tyr
NM_001079804.2:c.1940G>A NP_001073272.1:p.Cys647Tyr
NM_001079804.3:c.1940G>A NP_001073272.1:p.Cys647Tyr
ENST00000302262.7:c.1940G>A ENSP00000305692.3:p.Cys647Tyr
ENST00000390015.7:c.1940G>A ENSP00000374665.3:p.Cys647Tyr
ENST00000570716.1:n.380G>A
ENST00000570803.6:c.1940G>A ENSP00000460543.2:p.Cys647Tyr
ENST00000572080.1:c.359G>A
ENST00000572080.2:c.*78G>A ENSP00000459972.2:n.*78G>A
ENST00000572803.1:n.554G>A
ENST00000577106.6:c.1940G>A ENSP00000458306.2:p.Cys647Tyr
XM_005257193.1:c.1940G>A XP_005257250.1:p.Cys647Tyr
XM_005257193.2:c.1940G>A XP_005257250.1:p.Cys647Tyr
XM_005257194.3:c.1940G>A XP_005257251.1:p.Cys647Tyr
XM_005257194.4:c.1940G>A XP_005257251.1:p.Cys647Tyr