Canonical Allele Identifier: CA2260527980

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538711A= , CM000679.2:g.42538711A=	GRCh38
NC_000017.10:g.40690729A= , CM000679.1:g.40690729A=	GRCh37
NC_000017.9:g.37944255A=	NCBI36
NG_011552.1:g.7779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.720A= MANE Select	ENSP00000225927.1:p.Pro240=
ENST00000225927.6:c.720A=	ENSP00000225927.1:p.Pro240=
ENST00000586516.5:c.322A=
ENST00000591587.1:c.315A=	ENSP00000467836.1:p.Pro105=
NM_000263.3:c.720A=	NP_000254.2:p.Pro240=
XM_006721920.2:c.-23A=	XP_006721983.1:n.-23A=
XM_011524840.1:c.-23A=	XP_011523142.1:n.-23A=
XM_017024687.1:c.-23A=	XP_016880176.1:n.-23A=
XM_024450771.1:c.777A=	XP_024306539.1:p.Pro259=
XM_024450772.1:c.-23A=	XP_024306540.1:n.-23A=
NM_000263.4:c.720A= MANE Select	NP_000254.2:p.Pro240=