Canonical Allele Identifier: CA2260527817

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538354G= , CM000679.2:g.42538354G=	GRCh38
NC_000017.10:g.40690372G= , CM000679.1:g.40690372G=	GRCh37
NC_000017.9:g.37943898G=	NCBI36
NG_011552.1:g.7422G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.547G= MANE Select	ENSP00000225927.1:p.Gly183=
ENST00000225927.6:c.547G=	ENSP00000225927.1:p.Gly183=
ENST00000586516.5:c.149G=
ENST00000590358.1:c.235G=	ENSP00000466892.1:p.Gly79=
ENST00000591587.1:c.142G=	ENSP00000467836.1:p.Gly48=
NM_000263.3:c.547G=	NP_000254.2:p.Gly183=
XM_006721920.2:c.-196G=	XP_006721983.1:n.-196G=
XM_011524840.1:c.-196G=	XP_011523142.1:n.-196G=
XM_017024687.1:c.-196G=	XP_016880176.1:n.-196G=
XM_024450771.1:c.604G=	XP_024306539.1:p.Gly202=
XM_024450772.1:c.-196G=	XP_024306540.1:n.-196G=
NM_000263.4:c.547G= MANE Select	NP_000254.2:p.Gly183=