Canonical Allele Identifier: CA500218614

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42543938-C-T
• MyVariant Identifiers: chr17:g.40695956C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543938C>T , CM000679.2:g.42543938C>T	GRCh38
NC_000017.10:g.40695956C>T , CM000679.1:g.40695956C>T	GRCh37
NC_000017.9:g.37949482C>T	NCBI36
NG_011552.1:g.13006C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.1932C>T MANE Select	ENSP00000225927.1:p.Tyr644=
ENST00000225927.6:c.1932C>T	ENSP00000225927.1:p.Tyr644=
ENST00000591587.1:c.1270C>T	ENSP00000467836.1:n.1270C>T
NM_000263.3:c.1932C>T	NP_000254.2:p.Tyr644=
XM_006721920.2:c.1101C>T	XP_006721983.1:p.Tyr367=
XM_011524840.1:c.933C>T	XP_011523142.1:p.Tyr311=
XM_017024687.1:c.1101C>T	XP_016880176.1:p.Tyr367=
XM_024450771.1:c.1989C>T	XP_024306539.1:p.Tyr663=
XM_024450772.1:c.933C>T	XP_024306540.1:p.Tyr311=
NM_000263.4:c.1932C>T MANE Select	NP_000254.2:p.Tyr644=