Canonical Allele Identifier: CA626218578
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs1408078174

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42538628C>T , CM000679.2:g.42538628C>T GRCh38
NC_000017.10:g.40690646C>T , CM000679.1:g.40690646C>T GRCh37
NC_000017.9:g.37944172C>T NCBI36
NG_011552.1:g.7696C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.679-42C>T MANE Select ENSP00000225927.1:n.679-42C>T
ENST00000225927.6:c.679-42C>T ENSP00000225927.1:n.679-42C>T
ENST00000586516.5:c.281-42C>T
ENST00000591587.1:c.274-42C>T ENSP00000467836.1:n.274-42C>T
NM_000263.3:c.679-42C>T NP_000254.2:n.679-42C>T
XM_006721920.2:c.-64-42C>T XP_006721983.1:n.-64-42C>T
XM_011524840.1:c.-64-42C>T XP_011523142.1:n.-64-42C>T
XM_017024687.1:c.-64-42C>T XP_016880176.1:n.-64-42C>T
XM_024450771.1:c.736-42C>T XP_024306539.1:n.736-42C>T
XM_024450772.1:c.-64-42C>T XP_024306540.1:n.-64-42C>T
NM_000263.4:c.679-42C>T MANE Select NP_000254.2:n.679-42C>T