Canonical Allele Identifier: CA399601982

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695373A>C (hg19) ; chr17:g.42543355A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543355A>C , CM000679.2:g.42543355A>C	GRCh38
NC_000017.10:g.40695373A>C , CM000679.1:g.40695373A>C	GRCh37
NC_000017.9:g.37948899A>C	NCBI36
NG_011552.1:g.12423A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1349A>C MANE Select	ENSP00000225927.1:p.Gln450Pro
ENST00000225927.6:c.1349A>C	ENSP00000225927.1:p.Gln450Pro
ENST00000591587.1:c.687A>C	ENSP00000467836.1:n.687A>C
ENST00000592454.1:c.388A>C
NM_000263.3:c.1349A>C	NP_000254.2:p.Gln450Pro
XM_006721920.2:c.518A>C	XP_006721983.1:p.Gln173Pro
XM_011524840.1:c.350A>C	XP_011523142.1:p.Gln117Pro
XM_017024687.1:c.518A>C	XP_016880176.1:p.Gln173Pro
XM_024450771.1:c.1406A>C	XP_024306539.1:p.Gln469Pro
XM_024450772.1:c.350A>C	XP_024306540.1:p.Gln117Pro
NM_000263.4:c.1349A>C MANE Select	NP_000254.2:p.Gln450Pro