Canonical Allele Identifier: CA399595059
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536318G>A , CM000679.2:g.42536318G>A GRCh38
NC_000017.10:g.40688336G>A , CM000679.1:g.40688336G>A GRCh37
NC_000017.9:g.37941862G>A NCBI36
NG_011552.1:g.5386G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225927.7:c.46G>A MANE Select ENSP00000225927.1:p.Ala16Thr
ENST00000225927.6:c.46G>A ENSP00000225927.1:p.Ala16Thr
NM_000263.3:c.46G>A NP_000254.2:p.Ala16Thr
XM_024450771.1:c.46G>A XP_024306539.1:p.Ala16Thr
NM_000263.4:c.46G>A MANE Select NP_000254.2:p.Ala16Thr