Canonical Allele Identifier: CA2260530700

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544279G= , CM000679.2:g.42544279G=	GRCh38
NC_000017.10:g.40696297G= , CM000679.1:g.40696297G=	GRCh37
NC_000017.9:g.37949823G=	NCBI36
NG_011552.1:g.13347G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.*41G= MANE Select	ENSP00000225927.1:n.*41G=
ENST00000225927.6:c.*41G=	ENSP00000225927.1:n.*41G=
NM_000263.3:c.*41G=	NP_000254.2:n.*41G=
XM_006721920.2:c.*41G=	XP_006721983.1:n.*41G=
XM_011524840.1:c.*41G=	XP_011523142.1:n.*41G=
XM_017024687.1:c.*41G=	XP_016880176.1:n.*41G=
XM_024450771.1:c.*41G=	XP_024306539.1:n.*41G=
XM_024450772.1:c.*41G=	XP_024306540.1:n.*41G=
NM_000263.4:c.*41G= MANE Select	NP_000254.2:n.*41G=