Canonical Allele Identifier: CA401362459
Gene: GAA HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.78079656G>C (hg19) chr17:g.80105857G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105857G>C , CM000679.2:g.80105857G>C GRCh38
NC_000017.10:g.78079656G>C , CM000679.1:g.78079656G>C GRCh37
NC_000017.9:g.75694251G>C NCBI36
NG_009822.1:g.9302G>C , LRG_673:g.9302G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.655G>C ENSP00000460543.2:p.Gly219Arg
ENST00000572080.2:c.655G>C ENSP00000459972.2:p.Gly219Arg
ENST00000577106.6:c.655G>C ENSP00000458306.2:p.Gly219Arg
ENST00000302262.8:c.655G>C MANE Select ENSP00000305692.3:p.Gly219Arg
ENST00000302262.7:c.655G>C ENSP00000305692.3:p.Gly219Arg
ENST00000390015.7:c.655G>C ENSP00000374665.3:p.Gly219Arg
ENST00000570803.5:c.655G>C ENSP00000460543.1:p.Gly219Arg
NM_000152.3:c.655G>C , LRG_673t1:c.655G>C NP_000143.2:p.Gly219Arg
NM_001079803.1:c.655G>C NP_001073271.1:p.Gly219Arg
NM_001079804.1:c.655G>C NP_001073272.1:p.Gly219Arg
XM_005257193.1:c.655G>C XP_005257250.1:p.Gly219Arg
XM_005257194.3:c.655G>C XP_005257251.1:p.Gly219Arg
NM_000152.4:c.655G>C NP_000143.2:p.Gly219Arg
NM_001079803.2:c.655G>C NP_001073271.1:p.Gly219Arg
NM_001079804.2:c.655G>C NP_001073272.1:p.Gly219Arg
XM_005257193.2:c.655G>C XP_005257250.1:p.Gly219Arg
XM_005257194.4:c.655G>C XP_005257251.1:p.Gly219Arg
NM_000152.5:c.655G>C MANE Select NP_000143.2:p.Gly219Arg
NM_001079803.3:c.655G>C NP_001073271.1:p.Gly219Arg
NM_001079804.3:c.655G>C NP_001073272.1:p.Gly219Arg
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