Canonical Allele Identifier: CA399598929

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690712T>A (hg19) ; chr17:g.42538694T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538694T>A , CM000679.2:g.42538694T>A	GRCh38
NC_000017.10:g.40690712T>A , CM000679.1:g.40690712T>A	GRCh37
NC_000017.9:g.37944238T>A	NCBI36
NG_011552.1:g.7762T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.703T>A MANE Select	ENSP00000225927.1:p.Ser235Thr
ENST00000225927.6:c.703T>A	ENSP00000225927.1:p.Ser235Thr
ENST00000586516.5:c.305T>A
ENST00000591587.1:c.298T>A	ENSP00000467836.1:p.Ser100Thr
NM_000263.3:c.703T>A	NP_000254.2:p.Ser235Thr
XM_006721920.2:c.-40T>A	XP_006721983.1:n.-40T>A
XM_011524840.1:c.-40T>A	XP_011523142.1:n.-40T>A
XM_017024687.1:c.-40T>A	XP_016880176.1:n.-40T>A
XM_024450771.1:c.760T>A	XP_024306539.1:p.Ser254Thr
XM_024450772.1:c.-40T>A	XP_024306540.1:n.-40T>A
NM_000263.4:c.703T>A MANE Select	NP_000254.2:p.Ser235Thr