Canonical Allele Identifier: CA2260527975

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538701G= , CM000679.2:g.42538701G=	GRCh38
NC_000017.10:g.40690719G= , CM000679.1:g.40690719G=	GRCh37
NC_000017.9:g.37944245G=	NCBI36
NG_011552.1:g.7769G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.710G= MANE Select	ENSP00000225927.1:p.Gly237=
ENST00000225927.6:c.710G=	ENSP00000225927.1:p.Gly237=
ENST00000586516.5:c.312G=
ENST00000591587.1:c.305G=	ENSP00000467836.1:p.Gly102=
NM_000263.3:c.710G=	NP_000254.2:p.Gly237=
XM_006721920.2:c.-33G=	XP_006721983.1:n.-33G=
XM_011524840.1:c.-33G=	XP_011523142.1:n.-33G=
XM_017024687.1:c.-33G=	XP_016880176.1:n.-33G=
XM_024450771.1:c.767G=	XP_024306539.1:p.Gly256=
XM_024450772.1:c.-33G=	XP_024306540.1:n.-33G=
NM_000263.4:c.710G= MANE Select	NP_000254.2:p.Gly237=