Canonical Allele Identifier: CA399601829

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695334C>A (hg19) ; chr17:g.42543316C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543316C>A , CM000679.2:g.42543316C>A	GRCh38
NC_000017.10:g.40695334C>A , CM000679.1:g.40695334C>A	GRCh37
NC_000017.9:g.37948860C>A	NCBI36
NG_011552.1:g.12384C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1310C>A MANE Select	ENSP00000225927.1:p.Thr437Asn
ENST00000225927.6:c.1310C>A	ENSP00000225927.1:p.Thr437Asn
ENST00000591587.1:c.648C>A	ENSP00000467836.1:n.648C>A
ENST00000592454.1:c.349C>A
NM_000263.3:c.1310C>A	NP_000254.2:p.Thr437Asn
XM_006721920.2:c.479C>A	XP_006721983.1:p.Thr160Asn
XM_011524840.1:c.311C>A	XP_011523142.1:p.Thr104Asn
XM_017024687.1:c.479C>A	XP_016880176.1:p.Thr160Asn
XM_024450771.1:c.1367C>A	XP_024306539.1:p.Thr456Asn
XM_024450772.1:c.311C>A	XP_024306540.1:p.Thr104Asn
NM_000263.4:c.1310C>A MANE Select	NP_000254.2:p.Thr437Asn