Canonical Allele Identifier: CA399605985
Community Standard Title: NM_000263.4(NAGLU):c.2045T>G (p.Leu682Arg)
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42544051T>G , CM000679.2:g.42544051T>G GRCh38
NC_000017.10:g.40696069T>G , CM000679.1:g.40696069T>G GRCh37
NC_000017.9:g.37949595T>G NCBI36
NG_011552.1:g.13119T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.2045T>G MANE Select NP_000254.2:p.Leu682Arg
ENST00000225927.7:c.2045T>G MANE Select ENSP00000225927.1:p.Leu682Arg
NM_000263.3:c.2045T>G NP_000254.2:p.Leu682Arg
ENST00000225927.6:c.2045T>G ENSP00000225927.1:p.Leu682Arg
ENST00000591587.1:c.1383T>G ENSP00000467836.1:n.1383T>G
XM_006721920.2:c.1214T>G XP_006721983.1:p.Leu405Arg
XM_011524840.1:c.1046T>G XP_011523142.1:p.Leu349Arg
XM_017024687.1:c.1214T>G XP_016880176.1:p.Leu405Arg
XM_024450771.1:c.2102T>G XP_024306539.1:p.Leu701Arg
XM_024450772.1:c.1046T>G XP_024306540.1:p.Leu349Arg