Canonical Allele Identifier: CA399601600

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695276G>C (hg19) ; chr17:g.42543258G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543258G>C , CM000679.2:g.42543258G>C	GRCh38
NC_000017.10:g.40695276G>C , CM000679.1:g.40695276G>C	GRCh37
NC_000017.9:g.37948802G>C	NCBI36
NG_011552.1:g.12326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1252G>C MANE Select	ENSP00000225927.1:p.Gly418Arg
ENST00000225927.6:c.1252G>C	ENSP00000225927.1:p.Gly418Arg
ENST00000591587.1:c.590G>C	ENSP00000467836.1:n.590G>C
ENST00000592454.1:c.291G>C
NM_000263.3:c.1252G>C	NP_000254.2:p.Gly418Arg
XM_006721920.2:c.421G>C	XP_006721983.1:p.Gly141Arg
XM_011524840.1:c.253G>C	XP_011523142.1:p.Gly85Arg
XM_017024687.1:c.421G>C	XP_016880176.1:p.Gly141Arg
XM_024450771.1:c.1309G>C	XP_024306539.1:p.Gly437Arg
XM_024450772.1:c.253G>C	XP_024306540.1:p.Gly85Arg
NM_000263.4:c.1252G>C MANE Select	NP_000254.2:p.Gly418Arg