Canonical Allele Identifier: CA399605696

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543979A>G , CM000679.2:g.42543979A>G	GRCh38
NC_000017.10:g.40695997A>G , CM000679.1:g.40695997A>G	GRCh37
NC_000017.9:g.37949523A>G	NCBI36
NG_011552.1:g.13047A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000263.4:c.1973A>G MANE Select	NP_000254.2:p.Tyr658Cys
ENST00000225927.7:c.1973A>G MANE Select	ENSP00000225927.1:p.Tyr658Cys
NM_000263.3:c.1973A>G	NP_000254.2:p.Tyr658Cys
ENST00000225927.6:c.1973A>G	ENSP00000225927.1:p.Tyr658Cys
ENST00000591587.1:c.1311A>G	ENSP00000467836.1:n.1311A>G
XM_006721920.2:c.1142A>G	XP_006721983.1:p.Tyr381Cys
XM_011524840.1:c.974A>G	XP_011523142.1:p.Tyr325Cys
XM_017024687.1:c.1142A>G	XP_016880176.1:p.Tyr381Cys
XM_024450771.1:c.2030A>G	XP_024306539.1:p.Tyr677Cys
XM_024450772.1:c.974A>G	XP_024306540.1:p.Tyr325Cys