Canonical Allele Identifier: CA2260527947

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538628C= , CM000679.2:g.42538628C=	GRCh38
NC_000017.10:g.40690646C= , CM000679.1:g.40690646C=	GRCh37
NC_000017.9:g.37944172C=	NCBI36
NG_011552.1:g.7696C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.679-42C= MANE Select	ENSP00000225927.1:n.679-42C=
ENST00000225927.6:c.679-42C=	ENSP00000225927.1:n.679-42C=
ENST00000586516.5:c.281-42C=
ENST00000591587.1:c.274-42C=	ENSP00000467836.1:n.274-42C=
NM_000263.3:c.679-42C=	NP_000254.2:n.679-42C=
XM_006721920.2:c.-64-42C=	XP_006721983.1:n.-64-42C=
XM_011524840.1:c.-64-42C=	XP_011523142.1:n.-64-42C=
XM_017024687.1:c.-64-42C=	XP_016880176.1:n.-64-42C=
XM_024450771.1:c.736-42C=	XP_024306539.1:n.736-42C=
XM_024450772.1:c.-64-42C=	XP_024306540.1:n.-64-42C=
NM_000263.4:c.679-42C= MANE Select	NP_000254.2:n.679-42C=