Canonical Allele Identifier: CA399606031

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40696081T>A (hg19) ; chr17:g.42544063T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544063T>A , CM000679.2:g.42544063T>A	GRCh38
NC_000017.10:g.40696081T>A , CM000679.1:g.40696081T>A	GRCh37
NC_000017.9:g.37949607T>A	NCBI36
NG_011552.1:g.13131T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2057T>A MANE Select	ENSP00000225927.1:p.Val686Glu
ENST00000225927.6:c.2057T>A	ENSP00000225927.1:p.Val686Glu
ENST00000591587.1:c.1395T>A	ENSP00000467836.1:n.1395T>A
NM_000263.3:c.2057T>A	NP_000254.2:p.Val686Glu
XM_006721920.2:c.1226T>A	XP_006721983.1:p.Val409Glu
XM_011524840.1:c.1058T>A	XP_011523142.1:p.Val353Glu
XM_017024687.1:c.1226T>A	XP_016880176.1:p.Val409Glu
XM_024450771.1:c.2114T>A	XP_024306539.1:p.Val705Glu
XM_024450772.1:c.1058T>A	XP_024306540.1:p.Val353Glu
NM_000263.4:c.2057T>A MANE Select	NP_000254.2:p.Val686Glu