Canonical Allele Identifier: CA500217600

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40696160G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544142G>A , CM000679.2:g.42544142G>A	GRCh38
NC_000017.10:g.40696160G>A , CM000679.1:g.40696160G>A	GRCh37
NC_000017.9:g.37949686G>A	NCBI36
NG_011552.1:g.13210G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2136G>A MANE Select	ENSP00000225927.1:p.Lys712=
ENST00000225927.6:c.2136G>A	ENSP00000225927.1:p.Lys712=
ENST00000591587.1:c.1474G>A	ENSP00000467836.1:n.1474G>A
NM_000263.3:c.2136G>A	NP_000254.2:p.Lys712=
XM_006721920.2:c.1305G>A	XP_006721983.1:p.Lys435=
XM_011524840.1:c.1137G>A	XP_011523142.1:p.Lys379=
XM_017024687.1:c.1305G>A	XP_016880176.1:p.Lys435=
XM_024450771.1:c.2193G>A	XP_024306539.1:p.Lys731=
XM_024450772.1:c.1137G>A	XP_024306540.1:p.Lys379=
NM_000263.4:c.2136G>A MANE Select	NP_000254.2:p.Lys712=