Canonical Allele Identifier: CA399606512

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42544224-G-T
• MyVariant Identifiers: chr17:g.40696242G>T (hg19) ; chr17:g.42544224G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544224G>T , CM000679.2:g.42544224G>T	GRCh38
NC_000017.10:g.40696242G>T , CM000679.1:g.40696242G>T	GRCh37
NC_000017.9:g.37949768G>T	NCBI36
NG_011552.1:g.13292G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2218G>T MANE Select	ENSP00000225927.1:p.Ala740Ser
ENST00000225927.6:c.2218G>T	ENSP00000225927.1:p.Ala740Ser
NM_000263.3:c.2218G>T	NP_000254.2:p.Ala740Ser
XM_006721920.2:c.1387G>T	XP_006721983.1:p.Ala463Ser
XM_011524840.1:c.1219G>T	XP_011523142.1:p.Ala407Ser
XM_017024687.1:c.1387G>T	XP_016880176.1:p.Ala463Ser
XM_024450771.1:c.2275G>T	XP_024306539.1:p.Ala759Ser
XM_024450772.1:c.1219G>T	XP_024306540.1:p.Ala407Ser
NM_000263.4:c.2218G>T MANE Select	NP_000254.2:p.Ala740Ser