Canonical Allele Identifier: CA399605419

Gene: NAGLU

Linked Data

• dbSNP Id: rs74729489
• gnomAD v2: 17-40695922-C-T
• MyVariant Identifiers: chr17:g.40695922C>T (hg19) ; chr17:g.42543904C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543904C>T , CM000679.2:g.42543904C>T	GRCh38
NC_000017.10:g.40695922C>T , CM000679.1:g.40695922C>T	GRCh37
NC_000017.9:g.37949448C>T	NCBI36
NG_011552.1:g.12972C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1898C>T MANE Select	ENSP00000225927.1:p.Ala633Val
ENST00000225927.6:c.1898C>T	ENSP00000225927.1:p.Ala633Val
ENST00000591587.1:c.1236C>T	ENSP00000467836.1:n.1236C>T
NM_000263.3:c.1898C>T	NP_000254.2:p.Ala633Val
XM_006721920.2:c.1067C>T	XP_006721983.1:p.Ala356Val
XM_011524840.1:c.899C>T	XP_011523142.1:p.Ala300Val
XM_017024687.1:c.1067C>T	XP_016880176.1:p.Ala356Val
XM_024450771.1:c.1955C>T	XP_024306539.1:p.Ala652Val
XM_024450772.1:c.899C>T	XP_024306540.1:p.Ala300Val
NM_000263.4:c.1898C>T MANE Select	NP_000254.2:p.Ala633Val