Canonical Allele Identifier: CA399604926

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695827G>C (hg19) ; chr17:g.42543809G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543809G>C , CM000679.2:g.42543809G>C	GRCh38
NC_000017.10:g.40695827G>C , CM000679.1:g.40695827G>C	GRCh37
NC_000017.9:g.37949353G>C	NCBI36
NG_011552.1:g.12877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1803G>C MANE Select	ENSP00000225927.1:p.Glu601Asp
ENST00000225927.6:c.1803G>C	ENSP00000225927.1:p.Glu601Asp
ENST00000591587.1:c.1141G>C	ENSP00000467836.1:n.1141G>C
NM_000263.3:c.1803G>C	NP_000254.2:p.Glu601Asp
XM_006721920.2:c.972G>C	XP_006721983.1:p.Glu324Asp
XM_011524840.1:c.804G>C	XP_011523142.1:p.Glu268Asp
XM_017024687.1:c.972G>C	XP_016880176.1:p.Glu324Asp
XM_024450771.1:c.1860G>C	XP_024306539.1:p.Glu620Asp
XM_024450772.1:c.804G>C	XP_024306540.1:p.Glu268Asp
NM_000263.4:c.1803G>C MANE Select	NP_000254.2:p.Glu601Asp