Canonical Allele Identifier: CA2260527919

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538583_42538584delinsCG , CM000679.2:g.42538583_42538584delinsCG	GRCh38
NC_000017.10:g.40690601_40690602delinsCG , CM000679.1:g.40690601_40690602delinsCG	GRCh37
NC_000017.9:g.37944127_37944128delinsCG	NCBI36
NG_011552.1:g.7651_7652delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.679-87_679-86delinsCG MANE Select	ENSP00000225927.1:n.679-87_679-86delinsCG
ENST00000225927.6:c.679-87_679-86delinsCG	ENSP00000225927.1:n.679-87_679-86delinsCG
ENST00000586516.5:c.281-87_281-86delinsCG
ENST00000591587.1:c.274-87_274-86delinsCG	ENSP00000467836.1:n.274-87_274-86delinsCG
NM_000263.3:c.679-87_679-86delinsCG	NP_000254.2:n.679-87_679-86delinsCG
XM_006721920.2:c.-64-87_-64-86delinsCG	XP_006721983.1:n.-64-87_-64-86delinsCG
XM_011524840.1:c.-64-87_-64-86delinsCG	XP_011523142.1:n.-64-87_-64-86delinsCG
XM_017024687.1:c.-64-87_-64-86delinsCG	XP_016880176.1:n.-64-87_-64-86delinsCG
XM_024450771.1:c.736-87_736-86delinsCG	XP_024306539.1:n.736-87_736-86delinsCG
XM_024450772.1:c.-64-87_-64-86delinsCG	XP_024306540.1:n.-64-87_-64-86delinsCG
NM_000263.4:c.679-87_679-86delinsCG MANE Select	NP_000254.2:n.679-87_679-86delinsCG