Canonical Allele Identifier: CA399598949

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42538700-G-C
• MyVariant Identifiers: chr17:g.40690718G>C (hg19) ; chr17:g.42538700G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538700G>C , CM000679.2:g.42538700G>C	GRCh38
NC_000017.10:g.40690718G>C , CM000679.1:g.40690718G>C	GRCh37
NC_000017.9:g.37944244G>C	NCBI36
NG_011552.1:g.7768G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.709G>C MANE Select	ENSP00000225927.1:p.Gly237Arg
ENST00000225927.6:c.709G>C	ENSP00000225927.1:p.Gly237Arg
ENST00000586516.5:c.311G>C
ENST00000591587.1:c.304G>C	ENSP00000467836.1:p.Gly102Arg
NM_000263.3:c.709G>C	NP_000254.2:p.Gly237Arg
XM_006721920.2:c.-34G>C	XP_006721983.1:n.-34G>C
XM_011524840.1:c.-34G>C	XP_011523142.1:n.-34G>C
XM_017024687.1:c.-34G>C	XP_016880176.1:n.-34G>C
XM_024450771.1:c.766G>C	XP_024306539.1:p.Gly256Arg
XM_024450772.1:c.-34G>C	XP_024306540.1:n.-34G>C
NM_000263.4:c.709G>C MANE Select	NP_000254.2:p.Gly237Arg