Canonical Allele Identifier: CA399601806

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695328A>T (hg19) ; chr17:g.42543310A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543310A>T , CM000679.2:g.42543310A>T	GRCh38
NC_000017.10:g.40695328A>T , CM000679.1:g.40695328A>T	GRCh37
NC_000017.9:g.37948854A>T	NCBI36
NG_011552.1:g.12378A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1304A>T MANE Select	ENSP00000225927.1:p.Asn435Ile
ENST00000225927.6:c.1304A>T	ENSP00000225927.1:p.Asn435Ile
ENST00000591587.1:c.642A>T	ENSP00000467836.1:n.642A>T
ENST00000592454.1:c.343A>T
NM_000263.3:c.1304A>T	NP_000254.2:p.Asn435Ile
XM_006721920.2:c.473A>T	XP_006721983.1:p.Asn158Ile
XM_011524840.1:c.305A>T	XP_011523142.1:p.Asn102Ile
XM_017024687.1:c.473A>T	XP_016880176.1:p.Asn158Ile
XM_024450771.1:c.1361A>T	XP_024306539.1:p.Asn454Ile
XM_024450772.1:c.305A>T	XP_024306540.1:p.Asn102Ile
NM_000263.4:c.1304A>T MANE Select	NP_000254.2:p.Asn435Ile