Canonical Allele Identifier: CA658824779
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 553981
ClinVar RCV Id: RCV000669528
dbSNP Id: rs1555599619
MyVariant Identifiers: chr17:g.80107619dup (hg38)
ERepo: CA658824779/MONDO:0009290/010
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80107619dup , CM000679.2:g.80107619dup GRCh38
NC_000017.10:g.78081418dup , CM000679.1:g.78081418dup GRCh37
NC_000017.9:g.75696013dup NCBI36
NG_009822.1:g.11064dup , LRG_673:g.11064dup

Transcript Alleles

HGVS Amino-acid change
ENST00000570803.6:c.755dup ENSP00000460543.2:p.Pro253AlafsTer?
ENST00000572080.2:c.755dup ENSP00000459972.2:p.Pro253AlafsTer?
ENST00000577106.6:c.755dup ENSP00000458306.2:p.Pro253AlafsTer?
ENST00000302262.8:c.755dup MANE Select ENSP00000305692.3:p.Pro253AlafsTer?
ENST00000302262.7:c.755dup ENSP00000305692.3:p.Pro253AlafsTer?
ENST00000390015.7:c.755dup ENSP00000374665.3:p.Pro253AlafsTer?
ENST00000570803.5:c.755dup ENSP00000460543.1:p.Pro253AlafsTer?
NM_000152.3:c.755dup , LRG_673t1:c.755dup NP_000143.2:p.Pro253AlafsTer?
NM_001079803.1:c.755dup NP_001073271.1:p.Pro253AlafsTer?
NM_001079804.1:c.755dup NP_001073272.1:p.Pro253AlafsTer?
XM_005257193.1:c.755dup XP_005257250.1:p.Pro253AlafsTer?
XM_005257194.3:c.755dup XP_005257251.1:p.Pro253AlafsTer?
NM_000152.4:c.755dup NP_000143.2:p.Pro253AlafsTer?
NM_001079803.2:c.755dup NP_001073271.1:p.Pro253AlafsTer?
NM_001079804.2:c.755dup NP_001073272.1:p.Pro253AlafsTer?
XM_005257193.2:c.755dup XP_005257250.1:p.Pro253AlafsTer?
XM_005257194.4:c.755dup XP_005257251.1:p.Pro253AlafsTer?
NM_000152.5:c.755dup MANE Select NP_000143.2:p.Pro253AlafsTer?
NM_001079803.3:c.755dup NP_001073271.1:p.Pro253AlafsTer?
NM_001079804.3:c.755dup NP_001073272.1:p.Pro253AlafsTer?
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