Canonical Allele Identifier: CA500216319

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690386A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538368A>C , CM000679.2:g.42538368A>C	GRCh38
NC_000017.10:g.40690386A>C , CM000679.1:g.40690386A>C	GRCh37
NC_000017.9:g.37943912A>C	NCBI36
NG_011552.1:g.7436A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.561A>C MANE Select	ENSP00000225927.1:p.Ala187=
ENST00000225927.6:c.561A>C	ENSP00000225927.1:p.Ala187=
ENST00000586516.5:c.163A>C
ENST00000591587.1:c.156A>C	ENSP00000467836.1:p.Ala52=
NM_000263.3:c.561A>C	NP_000254.2:p.Ala187=
XM_006721920.2:c.-182A>C	XP_006721983.1:n.-182A>C
XM_011524840.1:c.-182A>C	XP_011523142.1:n.-182A>C
XM_017024687.1:c.-182A>C	XP_016880176.1:n.-182A>C
XM_024450771.1:c.618A>C	XP_024306539.1:p.Ala206=
XM_024450772.1:c.-182A>C	XP_024306540.1:n.-182A>C
NM_000263.4:c.561A>C MANE Select	NP_000254.2:p.Ala187=