Canonical Allele Identifier: CA401360566
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2139403
ClinVar RCV Id: RCV003070816
dbSNP Id: rs1470933192
MyVariant Identifiers: chr17:g.78078649C>G (hg19) chr17:g.80104850C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80104850C>G , CM000679.2:g.80104850C>G GRCh38
NC_000017.10:g.78078649C>G , CM000679.1:g.78078649C>G GRCh37
NC_000017.9:g.75693244C>G NCBI36
NG_009822.1:g.8295C>G , LRG_673:g.8295C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.264C>G ENSP00000460543.2:p.Ser88Arg
ENST00000572080.2:c.264C>G ENSP00000459972.2:p.Ser88Arg
ENST00000577106.6:c.264C>G ENSP00000458306.2:p.Ser88Arg
ENST00000302262.8:c.264C>G MANE Select ENSP00000305692.3:p.Ser88Arg
ENST00000302262.7:c.264C>G ENSP00000305692.3:p.Ser88Arg
ENST00000390015.7:c.264C>G ENSP00000374665.3:p.Ser88Arg
ENST00000570803.5:c.264C>G ENSP00000460543.1:p.Ser88Arg
ENST00000577106.5:c.264C>G ENSP00000458306.1:p.Ser88Arg
NM_000152.3:c.264C>G , LRG_673t1:c.264C>G NP_000143.2:p.Ser88Arg
NM_001079803.1:c.264C>G NP_001073271.1:p.Ser88Arg
NM_001079804.1:c.264C>G NP_001073272.1:p.Ser88Arg
XM_005257193.1:c.264C>G XP_005257250.1:p.Ser88Arg
XM_005257194.3:c.264C>G XP_005257251.1:p.Ser88Arg
NM_000152.4:c.264C>G NP_000143.2:p.Ser88Arg
NM_001079803.2:c.264C>G NP_001073271.1:p.Ser88Arg
NM_001079804.2:c.264C>G NP_001073272.1:p.Ser88Arg
XM_005257193.2:c.264C>G XP_005257250.1:p.Ser88Arg
XM_005257194.4:c.264C>G XP_005257251.1:p.Ser88Arg
NM_000152.5:c.264C>G MANE Select NP_000143.2:p.Ser88Arg
NM_001079803.3:c.264C>G NP_001073271.1:p.Ser88Arg
NM_001079804.3:c.264C>G NP_001073272.1:p.Ser88Arg
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