Canonical Allele Identifier: CA2637965378
Gene: NAGLU HGNC NCBI

Linked Data

gnomAD v4: 17-42536241-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536242del , CM000679.2:g.42536242del GRCh38
NC_000017.10:g.40688260del , CM000679.1:g.40688260del GRCh37
NC_000017.9:g.37941786del NCBI36
NG_011552.1:g.5310del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-31del MANE Select ENSP00000225927.1:n.-31del
ENST00000225927.6:c.-31del ENSP00000225927.1:n.-31del
NM_000263.3:c.-31del NP_000254.2:n.-31del
XM_024450771.1:c.-31del XP_024306539.1:n.-31del
NM_000263.4:c.-31del MANE Select NP_000254.2:n.-31del
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