Canonical Allele Identifier: CA399598325

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538338G>A , CM000679.2:g.42538338G>A	GRCh38
NC_000017.10:g.40690356G>A , CM000679.1:g.40690356G>A	GRCh37
NC_000017.9:g.37943882G>A	NCBI36
NG_011552.1:g.7406G>A

Transcript Alleles

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