Canonical Allele Identifier: CA2260526811

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536547A= , CM000679.2:g.42536547A=	GRCh38
NC_000017.10:g.40688565A= , CM000679.1:g.40688565A=	GRCh37
NC_000017.9:g.37942091A=	NCBI36
NG_011552.1:g.5615A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.275A= MANE Select	ENSP00000225927.1:p.Tyr92=
ENST00000225927.6:c.275A=	ENSP00000225927.1:p.Tyr92=
ENST00000586516.5:c.25A=
ENST00000591587.1:c.18A=	ENSP00000467836.1:p.Leu6=
NM_000263.3:c.275A=	NP_000254.2:p.Tyr92=
XM_006721920.2:c.-468A=	XP_006721983.1:n.-468A=
XM_011524840.1:c.-468A=	XP_011523142.1:n.-468A=
XM_024450771.1:c.275A=	XP_024306539.1:p.Tyr92=
NM_000263.4:c.275A= MANE Select	NP_000254.2:p.Tyr92=