Canonical Allele Identifier: CA2260527802

Gene: NAGLU

Linked Data

• dbSNP Id: rs2092912376

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538319T>C , CM000679.2:g.42538319T>C	GRCh38
NC_000017.10:g.40690337T>C , CM000679.1:g.40690337T>C	GRCh37
NC_000017.9:g.37943863T>C	NCBI36
NG_011552.1:g.7387T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.532-20T>C MANE Select	ENSP00000225927.1:n.532-20T>C
ENST00000225927.6:c.532-20T>C	ENSP00000225927.1:n.532-20T>C
ENST00000586516.5:c.134-20T>C
ENST00000590358.1:c.220-20T>C	ENSP00000466892.1:n.220-20T>C
ENST00000591587.1:c.127-20T>C	ENSP00000467836.1:n.127-20T>C
NM_000263.3:c.532-20T>C	NP_000254.2:n.532-20T>C
XM_006721920.2:c.-211-20T>C	XP_006721983.1:n.-211-20T>C
XM_011524840.1:c.-211-20T>C	XP_011523142.1:n.-211-20T>C
XM_017024687.1:c.-211-20T>C	XP_016880176.1:n.-211-20T>C
XM_024450771.1:c.589-20T>C	XP_024306539.1:n.589-20T>C
XM_024450772.1:c.-211-20T>C	XP_024306540.1:n.-211-20T>C
NM_000263.4:c.532-20T>C MANE Select	NP_000254.2:n.532-20T>C