Canonical Allele Identifier: CA399599004

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690731T>G (hg19) ; chr17:g.42538713T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538713T>G , CM000679.2:g.42538713T>G	GRCh38
NC_000017.10:g.40690731T>G , CM000679.1:g.40690731T>G	GRCh37
NC_000017.9:g.37944257T>G	NCBI36
NG_011552.1:g.7781T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.722T>G MANE Select	ENSP00000225927.1:p.Val241Gly
ENST00000225927.6:c.722T>G	ENSP00000225927.1:p.Val241Gly
ENST00000586516.5:c.324T>G
ENST00000591587.1:c.317T>G	ENSP00000467836.1:p.Val106Gly
NM_000263.3:c.722T>G	NP_000254.2:p.Val241Gly
XM_006721920.2:c.-21T>G	XP_006721983.1:n.-21T>G
XM_011524840.1:c.-21T>G	XP_011523142.1:n.-21T>G
XM_017024687.1:c.-21T>G	XP_016880176.1:n.-21T>G
XM_024450771.1:c.779T>G	XP_024306539.1:p.Val260Gly
XM_024450772.1:c.-21T>G	XP_024306540.1:n.-21T>G
NM_000263.4:c.722T>G MANE Select	NP_000254.2:p.Val241Gly