Canonical Allele Identifier: CA399597902

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42537401C>G , CM000679.2:g.42537401C>G	GRCh38
NC_000017.10:g.40689419C>G , CM000679.1:g.40689419C>G	GRCh37
NC_000017.9:g.37942945C>G	NCBI36
NG_011552.1:g.6469C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000263.4:c.387C>G MANE Select	NP_000254.2:p.Tyr129Ter
ENST00000225927.7:c.387C>G MANE Select	ENSP00000225927.1:p.Tyr129Ter
NM_000263.3:c.387C>G	NP_000254.2:p.Tyr129Ter
ENST00000225927.6:c.387C>G	ENSP00000225927.1:p.Tyr129Ter
ENST00000586516.5:c.133+746C>G
ENST00000590358.1:c.75C>G	ENSP00000466892.1:p.Tyr25Ter
ENST00000591587.1:c.126+746C>G	ENSP00000467836.1:n.126+746C>G
XM_006721920.2:c.-356C>G	XP_006721983.1:n.-356C>G
XM_011524840.1:c.-356C>G	XP_011523142.1:n.-356C>G
XM_017024687.1:c.-356C>G	XP_016880176.1:n.-356C>G
XM_024450771.1:c.444C>G	XP_024306539.1:p.Tyr148Ter
XM_024450772.1:c.-356C>G	XP_024306540.1:n.-356C>G