Canonical Allele Identifier: CA399599006

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690733C>G (hg19) ; chr17:g.42538715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538715C>G , CM000679.2:g.42538715C>G	GRCh38
NC_000017.10:g.40690733C>G , CM000679.1:g.40690733C>G	GRCh37
NC_000017.9:g.37944259C>G	NCBI36
NG_011552.1:g.7783C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.724C>G MANE Select	ENSP00000225927.1:p.Leu242Val
ENST00000225927.6:c.724C>G	ENSP00000225927.1:p.Leu242Val
ENST00000586516.5:c.326C>G
ENST00000591587.1:c.319C>G	ENSP00000467836.1:p.Leu107Val
NM_000263.3:c.724C>G	NP_000254.2:p.Leu242Val
XM_006721920.2:c.-19C>G	XP_006721983.1:n.-19C>G
XM_011524840.1:c.-19C>G	XP_011523142.1:n.-19C>G
XM_017024687.1:c.-19C>G	XP_016880176.1:n.-19C>G
XM_024450771.1:c.781C>G	XP_024306539.1:p.Leu261Val
XM_024450772.1:c.-19C>G	XP_024306540.1:n.-19C>G
NM_000263.4:c.724C>G MANE Select	NP_000254.2:p.Leu242Val