Canonical Allele Identifier: CA399601094
Community Standard Title: NM_000263.4(NAGLU):c.1082G>T (p.Trp361Leu)
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543088G>T , CM000679.2:g.42543088G>T GRCh38
NC_000017.10:g.40695106G>T , CM000679.1:g.40695106G>T GRCh37
NC_000017.9:g.37948632G>T NCBI36
NG_011552.1:g.12156G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.1082G>T MANE Select NP_000254.2:p.Trp361Leu
ENST00000225927.7:c.1082G>T MANE Select ENSP00000225927.1:p.Trp361Leu
NM_000263.3:c.1082G>T NP_000254.2:p.Trp361Leu
ENST00000225927.6:c.1082G>T ENSP00000225927.1:p.Trp361Leu
ENST00000591587.1:c.420G>T ENSP00000467836.1:n.420G>T
ENST00000592454.1:c.121G>T
XM_006721920.2:c.251G>T XP_006721983.1:p.Trp84Leu
XM_011524840.1:c.83G>T XP_011523142.1:p.Trp28Leu
XM_017024687.1:c.251G>T XP_016880176.1:p.Trp84Leu
XM_024450771.1:c.1139G>T XP_024306539.1:p.Trp380Leu
XM_024450772.1:c.83G>T XP_024306540.1:p.Trp28Leu