Canonical Allele Identifier: CA399603996

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543499T>C , CM000679.2:g.42543499T>C	GRCh38
NC_000017.10:g.40695517T>C , CM000679.1:g.40695517T>C	GRCh37
NC_000017.9:g.37949043T>C	NCBI36
NG_011552.1:g.12567T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000263.4:c.1493T>C MANE Select	NP_000254.2:p.Leu498Pro
ENST00000225927.7:c.1493T>C MANE Select	ENSP00000225927.1:p.Leu498Pro
NM_000263.3:c.1493T>C	NP_000254.2:p.Leu498Pro
ENST00000225927.6:c.1493T>C	ENSP00000225927.1:p.Leu498Pro
ENST00000591587.1:c.831T>C	ENSP00000467836.1:n.831T>C
ENST00000592454.1:c.532T>C
XM_006721920.2:c.662T>C	XP_006721983.1:p.Leu221Pro
XM_011524840.1:c.494T>C	XP_011523142.1:p.Leu165Pro
XM_017024687.1:c.662T>C	XP_016880176.1:p.Leu221Pro
XM_024450771.1:c.1550T>C	XP_024306539.1:p.Leu517Pro
XM_024450772.1:c.494T>C	XP_024306540.1:p.Leu165Pro