Canonical Allele Identifier: CA399605611

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42543960-G-C
• MyVariant Identifiers: chr17:g.40695978G>C (hg19) ; chr17:g.42543960G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543960G>C , CM000679.2:g.42543960G>C	GRCh38
NC_000017.10:g.40695978G>C , CM000679.1:g.40695978G>C	GRCh37
NC_000017.9:g.37949504G>C	NCBI36
NG_011552.1:g.13028G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.1954G>C MANE Select	ENSP00000225927.1:p.Glu652Gln
ENST00000225927.6:c.1954G>C	ENSP00000225927.1:p.Glu652Gln
ENST00000591587.1:c.1292G>C	ENSP00000467836.1:n.1292G>C
NM_000263.3:c.1954G>C	NP_000254.2:p.Glu652Gln
XM_006721920.2:c.1123G>C	XP_006721983.1:p.Glu375Gln
XM_011524840.1:c.955G>C	XP_011523142.1:p.Glu319Gln
XM_017024687.1:c.1123G>C	XP_016880176.1:p.Glu375Gln
XM_024450771.1:c.2011G>C	XP_024306539.1:p.Glu671Gln
XM_024450772.1:c.955G>C	XP_024306540.1:p.Glu319Gln
NM_000263.4:c.1954G>C MANE Select	NP_000254.2:p.Glu652Gln