Canonical Allele Identifier: CA399599123

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690763G>C (hg19) ; chr17:g.42538745G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538745G>C , CM000679.2:g.42538745G>C	GRCh38
NC_000017.10:g.40690763G>C , CM000679.1:g.40690763G>C	GRCh37
NC_000017.9:g.37944289G>C	NCBI36
NG_011552.1:g.7813G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.754G>C MANE Select	ENSP00000225927.1:p.Ala252Pro
ENST00000225927.6:c.754G>C	ENSP00000225927.1:p.Ala252Pro
ENST00000586516.5:c.356G>C
ENST00000591587.1:c.349G>C	ENSP00000467836.1:p.Ala117Pro
NM_000263.3:c.754G>C	NP_000254.2:p.Ala252Pro
XM_006721920.2:c.12G>C	XP_006721983.1:p.Arg4Ser
XM_011524840.1:c.12G>C	XP_011523142.1:p.Arg4Ser
XM_017024687.1:c.12G>C	XP_016880176.1:p.Arg4Ser
XM_024450771.1:c.811G>C	XP_024306539.1:p.Ala271Pro
XM_024450772.1:c.12G>C	XP_024306540.1:p.Arg4Ser
NM_000263.4:c.754G>C MANE Select	NP_000254.2:p.Ala252Pro