Canonical Allele Identifier: CA8577101
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 1907752
ClinVar RCV Id: RCV002581033
dbSNP Id: rs756855449
ExAC: 17:40695836 G / A
gnomAD v2: 17-40695836-G-A
gnomAD v3: 17-42543818-G-A
gnomAD v4: 17-42543818-G-A
MyVariant Identifiers: chr17:g.40695836G>A (hg19) chr17:g.42543818G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543818G>A , CM000679.2:g.42543818G>A GRCh38
NC_000017.10:g.40695836G>A , CM000679.1:g.40695836G>A GRCh37
NC_000017.9:g.37949362G>A NCBI36
NG_011552.1:g.12886G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.1812G>A MANE Select ENSP00000225927.1:p.Pro604=
ENST00000225927.6:c.1812G>A ENSP00000225927.1:p.Pro604=
ENST00000591587.1:c.1150G>A ENSP00000467836.1:n.1150G>A
NM_000263.3:c.1812G>A NP_000254.2:p.Pro604=
XM_006721920.2:c.981G>A XP_006721983.1:p.Pro327=
XM_011524840.1:c.813G>A XP_011523142.1:p.Pro271=
XM_017024687.1:c.981G>A XP_016880176.1:p.Pro327=
XM_024450771.1:c.1869G>A XP_024306539.1:p.Pro623=
XM_024450772.1:c.813G>A XP_024306540.1:p.Pro271=
NM_000263.4:c.1812G>A MANE Select NP_000254.2:p.Pro604=
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