Canonical Allele Identifier: CA8815852
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1795875
ClinVar RCV Id: RCV002439685 RCV003102202
dbSNP Id: rs760016362
ExAC: 17:78092583 C / T
gnomAD v2: 17-78092583-C-T
gnomAD v4: 17-80118784-C-T
MyVariant Identifiers: chr17:g.78092583C>T (hg19) chr17:g.80118784C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118784C>T , CM000679.2:g.80118784C>T GRCh38
NC_000017.10:g.78092583C>T , CM000679.1:g.78092583C>T GRCh37
NC_000017.9:g.75707178C>T NCBI36
NG_009822.1:g.22229C>T , LRG_673:g.22229C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2778C>T ENSP00000460543.2:p.Phe926=
ENST00000572080.2:c.*916C>T ENSP00000459972.2:n.*916C>T
ENST00000577106.6:c.2778C>T ENSP00000458306.2:p.Phe926=
ENST00000302262.8:c.2778C>T MANE Select ENSP00000305692.3:p.Phe926=
ENST00000302262.7:c.2778C>T ENSP00000305692.3:p.Phe926=
ENST00000390015.7:c.2778C>T ENSP00000374665.3:p.Phe926=
ENST00000573556.1:n.731C>T
NM_000152.3:c.2778C>T , LRG_673t1:c.2778C>T NP_000143.2:p.Phe926=
NM_001079803.1:c.2778C>T NP_001073271.1:p.Phe926=
NM_001079804.1:c.2778C>T NP_001073272.1:p.Phe926=
XM_005257193.1:c.2778C>T XP_005257250.1:p.Phe926=
XM_005257194.3:c.2778C>T XP_005257251.1:p.Phe926=
NM_000152.4:c.2778C>T NP_000143.2:p.Phe926=
NM_001079803.2:c.2778C>T NP_001073271.1:p.Phe926=
NM_001079804.2:c.2778C>T NP_001073272.1:p.Phe926=
XM_005257193.2:c.2778C>T XP_005257250.1:p.Phe926=
XM_005257194.4:c.2778C>T XP_005257251.1:p.Phe926=
NM_000152.5:c.2778C>T MANE Select NP_000143.2:p.Phe926=
NM_001079803.3:c.2778C>T NP_001073271.1:p.Phe926=
NM_001079804.3:c.2778C>T NP_001073272.1:p.Phe926=
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