Canonical Allele Identifier: CA2260527973

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538699C= , CM000679.2:g.42538699C=	GRCh38
NC_000017.10:g.40690717C= , CM000679.1:g.40690717C=	GRCh37
NC_000017.9:g.37944243C=	NCBI36
NG_011552.1:g.7767C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.708C= MANE Select	ENSP00000225927.1:p.Phe236=
ENST00000225927.6:c.708C=	ENSP00000225927.1:p.Phe236=
ENST00000586516.5:c.310C=
ENST00000591587.1:c.303C=	ENSP00000467836.1:p.Phe101=
NM_000263.3:c.708C=	NP_000254.2:p.Phe236=
XM_006721920.2:c.-35C=	XP_006721983.1:n.-35C=
XM_011524840.1:c.-35C=	XP_011523142.1:n.-35C=
XM_017024687.1:c.-35C=	XP_016880176.1:n.-35C=
XM_024450771.1:c.765C=	XP_024306539.1:p.Phe255=
XM_024450772.1:c.-35C=	XP_024306540.1:n.-35C=
NM_000263.4:c.708C= MANE Select	NP_000254.2:p.Phe236=