Canonical Allele Identifier: CA399600410

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42541198-T-C
• MyVariant Identifiers: chr17:g.40693216T>C (hg19) ; chr17:g.42541198T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541198T>C , CM000679.2:g.42541198T>C	GRCh38
NC_000017.10:g.40693216T>C , CM000679.1:g.40693216T>C	GRCh37
NC_000017.9:g.37946742T>C	NCBI36
NG_011552.1:g.10266T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1013T>C MANE Select	ENSP00000225927.1:p.Met338Thr
ENST00000225927.6:c.1013T>C	ENSP00000225927.1:p.Met338Thr
ENST00000591587.1:c.360-1830T>C	ENSP00000467836.1:n.360-1830T>C
ENST00000592454.1:c.108T>C
NM_000263.3:c.1013T>C	NP_000254.2:p.Met338Thr
XM_006721920.2:c.182T>C	XP_006721983.1:p.Met61Thr
XM_011524840.1:c.23-1830T>C	XP_011523142.1:n.23-1830T>C
XM_017024687.1:c.182T>C	XP_016880176.1:p.Met61Thr
XM_024450771.1:c.1070T>C	XP_024306539.1:p.Met357Thr
XM_024450772.1:c.23-1830T>C	XP_024306540.1:n.23-1830T>C
NM_000263.4:c.1013T>C MANE Select	NP_000254.2:p.Met338Thr