Canonical Allele Identifier: CA8576888

Gene: NAGLU

Linked Data

• ClinVar Variation Id: 1027046
• ClinVar RCV Id: RCV001327591
• dbSNP Id: rs750625891
• ExAC: 17:40693051 C / T
• gnomAD v2: 17-40693051-C-T
• gnomAD v3: 17-42541033-C-T
• gnomAD v4: 17-42541033-C-T
• MyVariant Identifiers: chr17:g.40693051C>T (hg19) ; chr17:g.42541033C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541033C>T , CM000679.2:g.42541033C>T	GRCh38
NC_000017.10:g.40693051C>T , CM000679.1:g.40693051C>T	GRCh37
NC_000017.9:g.37946577C>T	NCBI36
NG_011552.1:g.10101C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.848C>T MANE Select	ENSP00000225927.1:p.Pro283Leu
ENST00000225927.6:c.848C>T	ENSP00000225927.1:p.Pro283Leu
ENST00000586516.5:c.450C>T
ENST00000591587.1:c.360-1995C>T	ENSP00000467836.1:n.360-1995C>T
NM_000263.3:c.848C>T	NP_000254.2:p.Pro283Leu
XM_006721920.2:c.23-6C>T	XP_006721983.1:n.23-6C>T
XM_011524840.1:c.23-1995C>T	XP_011523142.1:n.23-1995C>T
XM_017024687.1:c.23-6C>T	XP_016880176.1:n.23-6C>T
XM_024450771.1:c.905C>T	XP_024306539.1:p.Pro302Leu
XM_024450772.1:c.23-1995C>T	XP_024306540.1:n.23-1995C>T
NM_000263.4:c.848C>T MANE Select	NP_000254.2:p.Pro283Leu