Canonical Allele Identifier: CA500217230

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42543701-G-C
• MyVariant Identifiers: chr17:g.40695719G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543701G>C , CM000679.2:g.42543701G>C	GRCh38
NC_000017.10:g.40695719G>C , CM000679.1:g.40695719G>C	GRCh37
NC_000017.9:g.37949245G>C	NCBI36
NG_011552.1:g.12769G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1695G>C MANE Select	ENSP00000225927.1:p.Arg565=
ENST00000225927.6:c.1695G>C	ENSP00000225927.1:p.Arg565=
ENST00000591587.1:c.1033G>C	ENSP00000467836.1:n.1033G>C
NM_000263.3:c.1695G>C	NP_000254.2:p.Arg565=
XM_006721920.2:c.864G>C	XP_006721983.1:p.Arg288=
XM_011524840.1:c.696G>C	XP_011523142.1:p.Arg232=
XM_017024687.1:c.864G>C	XP_016880176.1:p.Arg288=
XM_024450771.1:c.1752G>C	XP_024306539.1:p.Arg584=
XM_024450772.1:c.696G>C	XP_024306540.1:p.Arg232=
NM_000263.4:c.1695G>C MANE Select	NP_000254.2:p.Arg565=