Canonical Allele Identifier: CA399598449

Gene: NAGLU

Linked Data

• dbSNP Id: rs1599255987
• MyVariant Identifiers: chr17:g.40690412C>A (hg19) ; chr17:g.42538394C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538394C>A , CM000679.2:g.42538394C>A	GRCh38
NC_000017.10:g.40690412C>A , CM000679.1:g.40690412C>A	GRCh37
NC_000017.9:g.37943938C>A	NCBI36
NG_011552.1:g.7462C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.587C>A MANE Select	ENSP00000225927.1:p.Pro196His
ENST00000225927.6:c.587C>A	ENSP00000225927.1:p.Pro196His
ENST00000586516.5:c.189C>A
ENST00000591587.1:c.182C>A	ENSP00000467836.1:p.Pro61His
NM_000263.3:c.587C>A	NP_000254.2:p.Pro196His
XM_006721920.2:c.-156C>A	XP_006721983.1:n.-156C>A
XM_011524840.1:c.-156C>A	XP_011523142.1:n.-156C>A
XM_017024687.1:c.-156C>A	XP_016880176.1:n.-156C>A
XM_024450771.1:c.644C>A	XP_024306539.1:p.Pro215His
XM_024450772.1:c.-156C>A	XP_024306540.1:n.-156C>A
NM_000263.4:c.587C>A MANE Select	NP_000254.2:p.Pro196His