Canonical Allele Identifier: CA399600388

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40693206T>G (hg19) ; chr17:g.42541188T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541188T>G , CM000679.2:g.42541188T>G	GRCh38
NC_000017.10:g.40693206T>G , CM000679.1:g.40693206T>G	GRCh37
NC_000017.9:g.37946732T>G	NCBI36
NG_011552.1:g.10256T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1003T>G MANE Select	ENSP00000225927.1:p.Tyr335Asp
ENST00000225927.6:c.1003T>G	ENSP00000225927.1:p.Tyr335Asp
ENST00000591587.1:c.360-1840T>G	ENSP00000467836.1:n.360-1840T>G
ENST00000592454.1:c.98T>G
NM_000263.3:c.1003T>G	NP_000254.2:p.Tyr335Asp
XM_006721920.2:c.172T>G	XP_006721983.1:p.Tyr58Asp
XM_011524840.1:c.23-1840T>G	XP_011523142.1:n.23-1840T>G
XM_017024687.1:c.172T>G	XP_016880176.1:p.Tyr58Asp
XM_024450771.1:c.1060T>G	XP_024306539.1:p.Tyr354Asp
XM_024450772.1:c.23-1840T>G	XP_024306540.1:n.23-1840T>G
NM_000263.4:c.1003T>G MANE Select	NP_000254.2:p.Tyr335Asp