Canonical Allele Identifier: CA399604459
Community Standard Title: NM_000263.4(NAGLU):c.1682T>C (p.Leu561Pro)
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543688T>C , CM000679.2:g.42543688T>C GRCh38
NC_000017.10:g.40695706T>C , CM000679.1:g.40695706T>C GRCh37
NC_000017.9:g.37949232T>C NCBI36
NG_011552.1:g.12756T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.1682T>C MANE Select NP_000254.2:p.Leu561Pro
ENST00000225927.7:c.1682T>C MANE Select ENSP00000225927.1:p.Leu561Pro
NM_000263.3:c.1682T>C NP_000254.2:p.Leu561Pro
ENST00000225927.6:c.1682T>C ENSP00000225927.1:p.Leu561Pro
ENST00000591587.1:c.1020T>C ENSP00000467836.1:n.1020T>C
XM_006721920.2:c.851T>C XP_006721983.1:p.Leu284Pro
XM_011524840.1:c.683T>C XP_011523142.1:p.Leu228Pro
XM_017024687.1:c.851T>C XP_016880176.1:p.Leu284Pro
XM_024450771.1:c.1739T>C XP_024306539.1:p.Leu580Pro
XM_024450772.1:c.683T>C XP_024306540.1:p.Leu228Pro