Canonical Allele Identifier: CA2260526941
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs2092907543

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536760C>T , CM000679.2:g.42536760C>T GRCh38
NC_000017.10:g.40688778C>T , CM000679.1:g.40688778C>T GRCh37
NC_000017.9:g.37942304C>T NCBI36
NG_011552.1:g.5828C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.383+105C>T MANE Select ENSP00000225927.1:n.383+105C>T
ENST00000225927.6:c.383+105C>T ENSP00000225927.1:n.383+105C>T
ENST00000586516.5:c.133+105C>T
ENST00000591587.1:c.126+105C>T ENSP00000467836.1:n.126+105C>T
NM_000263.3:c.383+105C>T NP_000254.2:n.383+105C>T
XM_006721920.2:c.-360+105C>T XP_006721983.1:n.-360+105C>T
XM_011524840.1:c.-360+105C>T XP_011523142.1:n.-360+105C>T
XM_024450771.1:c.384-57C>T XP_024306539.1:n.384-57C>T
NM_000263.4:c.383+105C>T MANE Select NP_000254.2:n.383+105C>T