Canonical Allele Identifier: CA399606457

Gene: NAGLU

Linked Data

• ClinVar Variation Id: 2010740
• ClinVar RCV Id: RCV002834219
• MyVariant Identifiers: chr17:g.40696229C>A (hg19) ; chr17:g.42544211C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544211C>A , CM000679.2:g.42544211C>A	GRCh38
NC_000017.10:g.40696229C>A , CM000679.1:g.40696229C>A	GRCh37
NC_000017.9:g.37949755C>A	NCBI36
NG_011552.1:g.13279C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2205C>A MANE Select	ENSP00000225927.1:p.Tyr735Ter
ENST00000225927.6:c.2205C>A	ENSP00000225927.1:p.Tyr735Ter
NM_000263.3:c.2205C>A	NP_000254.2:p.Tyr735Ter
XM_006721920.2:c.1374C>A	XP_006721983.1:p.Tyr458Ter
XM_011524840.1:c.1206C>A	XP_011523142.1:p.Tyr402Ter
XM_017024687.1:c.1374C>A	XP_016880176.1:p.Tyr458Ter
XM_024450771.1:c.2262C>A	XP_024306539.1:p.Tyr754Ter
XM_024450772.1:c.1206C>A	XP_024306540.1:p.Tyr402Ter
NM_000263.4:c.2205C>A MANE Select	NP_000254.2:p.Tyr735Ter