Canonical Allele Identifier: CA2260530699
Gene: NAGLU HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42544278A= , CM000679.2:g.42544278A= GRCh38
NC_000017.10:g.40696296A= , CM000679.1:g.40696296A= GRCh37
NC_000017.9:g.37949822A= NCBI36
NG_011552.1:g.13346A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.*40A= MANE Select ENSP00000225927.1:n.*40A=
ENST00000225927.6:c.*40A= ENSP00000225927.1:n.*40A=
NM_000263.3:c.*40A= NP_000254.2:n.*40A=
XM_006721920.2:c.*40A= XP_006721983.1:n.*40A=
XM_011524840.1:c.*40A= XP_011523142.1:n.*40A=
XM_017024687.1:c.*40A= XP_016880176.1:n.*40A=
XM_024450771.1:c.*40A= XP_024306539.1:n.*40A=
XM_024450772.1:c.*40A= XP_024306540.1:n.*40A=
NM_000263.4:c.*40A= MANE Select NP_000254.2:n.*40A=
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