Canonical Allele Identifier: CA772109867
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs1176620061
MyVariant Identifiers: chr17:g.40688748A>C (hg19) chr17:g.42536730A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536730A>C , CM000679.2:g.42536730A>C GRCh38
NC_000017.10:g.40688748A>C , CM000679.1:g.40688748A>C GRCh37
NC_000017.9:g.37942274A>C NCBI36
NG_011552.1:g.5798A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.383+75A>C MANE Select ENSP00000225927.1:n.383+75A>C
ENST00000225927.6:c.383+75A>C ENSP00000225927.1:n.383+75A>C
ENST00000586516.5:c.133+75A>C
ENST00000591587.1:c.126+75A>C ENSP00000467836.1:n.126+75A>C
NM_000263.3:c.383+75A>C NP_000254.2:n.383+75A>C
XM_006721920.2:c.-360+75A>C XP_006721983.1:n.-360+75A>C
XM_011524840.1:c.-360+75A>C XP_011523142.1:n.-360+75A>C
XM_024450771.1:c.383+75A>C XP_024306539.1:n.383+75A>C
NM_000263.4:c.383+75A>C MANE Select NP_000254.2:n.383+75A>C
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