Canonical Allele Identifier: CA2260527791

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538300A= , CM000679.2:g.42538300A=	GRCh38
NC_000017.10:g.40690318A= , CM000679.1:g.40690318A=	GRCh37
NC_000017.9:g.37943844A=	NCBI36
NG_011552.1:g.7368A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.532-39A= MANE Select	ENSP00000225927.1:n.532-39A=
ENST00000225927.6:c.532-39A=	ENSP00000225927.1:n.532-39A=
ENST00000586516.5:c.134-39A=
ENST00000590358.1:c.220-39A=	ENSP00000466892.1:n.220-39A=
ENST00000591587.1:c.127-39A=	ENSP00000467836.1:n.127-39A=
NM_000263.3:c.532-39A=	NP_000254.2:n.532-39A=
XM_006721920.2:c.-211-39A=	XP_006721983.1:n.-211-39A=
XM_011524840.1:c.-211-39A=	XP_011523142.1:n.-211-39A=
XM_017024687.1:c.-211-39A=	XP_016880176.1:n.-211-39A=
XM_024450771.1:c.589-39A=	XP_024306539.1:n.589-39A=
XM_024450772.1:c.-211-39A=	XP_024306540.1:n.-211-39A=
NM_000263.4:c.532-39A= MANE Select	NP_000254.2:n.532-39A=