Canonical Allele Identifier: CA2573154965
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1459200
ClinVar RCV Id: RCV001958884
dbSNP Id: rs2143866239
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80109992_80109993delinsTA , CM000679.2:g.80109992_80109993delinsTA GRCh38
NC_000017.10:g.78083791_78083792delinsTA , CM000679.1:g.78083791_78083792delinsTA GRCh37
NC_000017.9:g.75698386_75698387delinsTA NCBI36
NG_009822.1:g.13437_13438delinsTA , LRG_673:g.13437_13438delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.1374_1375delinsTA ENSP00000460543.2:p.Asp459Asn
ENST00000572080.2:c.1374_1375delinsTA ENSP00000459972.2:p.Asp459Asn
ENST00000577106.6:c.1374_1375delinsTA ENSP00000458306.2:p.Asp459Asn
ENST00000302262.8:c.1374_1375delinsTA MANE Select ENSP00000305692.3:p.Asp459Asn
ENST00000302262.7:c.1374_1375delinsTA ENSP00000305692.3:p.Asp459Asn
ENST00000390015.7:c.1374_1375delinsTA ENSP00000374665.3:p.Asp459Asn
NM_000152.3:c.1374_1375delinsTA , LRG_673t1:c.1374_1375delinsTA NP_000143.2:p.Asp459Asn
NM_001079803.1:c.1374_1375delinsTA NP_001073271.1:p.Asp459Asn
NM_001079804.1:c.1374_1375delinsTA NP_001073272.1:p.Asp459Asn
XM_005257193.1:c.1374_1375delinsTA XP_005257250.1:p.Asp459Asn
XM_005257194.3:c.1374_1375delinsTA XP_005257251.1:p.Asp459Asn
NM_000152.4:c.1374_1375delinsTA NP_000143.2:p.Asp459Asn
NM_001079803.2:c.1374_1375delinsTA NP_001073271.1:p.Asp459Asn
NM_001079804.2:c.1374_1375delinsTA NP_001073272.1:p.Asp459Asn
XM_005257193.2:c.1374_1375delinsTA XP_005257250.1:p.Asp459Asn
XM_005257194.4:c.1374_1375delinsTA XP_005257251.1:p.Asp459Asn
NM_000152.5:c.1374_1375delinsTA MANE Select NP_000143.2:p.Asp459Asn
NM_001079803.3:c.1374_1375delinsTA NP_001073271.1:p.Asp459Asn
NM_001079804.3:c.1374_1375delinsTA NP_001073272.1:p.Asp459Asn
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