Canonical Allele Identifier: CA399605418

Gene: NAGLU

Linked Data

• dbSNP Id: rs1599262002
• MyVariant Identifiers: chr17:g.40695921G>T (hg19) ; chr17:g.42543903G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543903G>T , CM000679.2:g.42543903G>T	GRCh38
NC_000017.10:g.40695921G>T , CM000679.1:g.40695921G>T	GRCh37
NC_000017.9:g.37949447G>T	NCBI36
NG_011552.1:g.12971G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1897G>T MANE Select	ENSP00000225927.1:p.Ala633Ser
ENST00000225927.6:c.1897G>T	ENSP00000225927.1:p.Ala633Ser
ENST00000591587.1:c.1235G>T	ENSP00000467836.1:n.1235G>T
NM_000263.3:c.1897G>T	NP_000254.2:p.Ala633Ser
XM_006721920.2:c.1066G>T	XP_006721983.1:p.Ala356Ser
XM_011524840.1:c.898G>T	XP_011523142.1:p.Ala300Ser
XM_017024687.1:c.1066G>T	XP_016880176.1:p.Ala356Ser
XM_024450771.1:c.1954G>T	XP_024306539.1:p.Ala652Ser
XM_024450772.1:c.898G>T	XP_024306540.1:p.Ala300Ser
NM_000263.4:c.1897G>T MANE Select	NP_000254.2:p.Ala633Ser