Canonical Allele Identifier: CA626218592

Gene: NAGLU

Linked Data

• dbSNP Id: rs1370819214
• gnomAD v2: 17-40692945-T-C
• gnomAD v3: 17-42540927-T-C
• gnomAD v4: 17-42540927-T-C
• MyVariant Identifiers: chr17:g.40692945T>C (hg19) ; chr17:g.42540927T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42540927T>C , CM000679.2:g.42540927T>C	GRCh38
NC_000017.10:g.40692945T>C , CM000679.1:g.40692945T>C	GRCh37
NC_000017.9:g.37946471T>C	NCBI36
NG_011552.1:g.9995T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.765-23T>C MANE Select	ENSP00000225927.1:n.765-23T>C
ENST00000225927.6:c.765-23T>C	ENSP00000225927.1:n.765-23T>C
ENST00000586516.5:c.367-23T>C
ENST00000591587.1:c.360-2101T>C	ENSP00000467836.1:n.360-2101T>C
NM_000263.3:c.765-23T>C	NP_000254.2:n.765-23T>C
XM_006721920.2:c.23-112T>C	XP_006721983.1:n.23-112T>C
XM_011524840.1:c.23-2101T>C	XP_011523142.1:n.23-2101T>C
XM_017024687.1:c.23-112T>C	XP_016880176.1:n.23-112T>C
XM_024450771.1:c.822-23T>C	XP_024306539.1:n.822-23T>C
XM_024450772.1:c.23-2101T>C	XP_024306540.1:n.23-2101T>C
NM_000263.4:c.765-23T>C MANE Select	NP_000254.2:n.765-23T>C