Canonical Allele Identifier: CA399606378

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40696213T>G (hg19) ; chr17:g.42544195T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544195T>G , CM000679.2:g.42544195T>G	GRCh38
NC_000017.10:g.40696213T>G , CM000679.1:g.40696213T>G	GRCh37
NC_000017.9:g.37949739T>G	NCBI36
NG_011552.1:g.13263T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2189T>G MANE Select	ENSP00000225927.1:p.Ile730Ser
ENST00000225927.6:c.2189T>G	ENSP00000225927.1:p.Ile730Ser
NM_000263.3:c.2189T>G	NP_000254.2:p.Ile730Ser
XM_006721920.2:c.1358T>G	XP_006721983.1:p.Ile453Ser
XM_011524840.1:c.1190T>G	XP_011523142.1:p.Ile397Ser
XM_017024687.1:c.1358T>G	XP_016880176.1:p.Ile453Ser
XM_024450771.1:c.2246T>G	XP_024306539.1:p.Ile749Ser
XM_024450772.1:c.1190T>G	XP_024306540.1:p.Ile397Ser
NM_000263.4:c.2189T>G MANE Select	NP_000254.2:p.Ile730Ser