Canonical Allele Identifier: CA780918045
Gene: NEDD4L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58316098T>A , CM000680.2:g.58316098T>A GRCh38
NC_000018.9:g.55983330T>A , CM000680.1:g.55983330T>A GRCh37
NC_000018.8:g.54134310T>A NCBI36
NG_029954.1:g.276721T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400345.8:c.348+66T>A MANE Select ENSP00000383199.2:n.348+66T>A
ENST00000635997.1:c.1185+66T>A ENSP00000490696.1:n.1185+66T>A
ENST00000674517.1:c.-16+66T>A ENSP00000501665.1:n.-16+66T>A
ENST00000674636.1:n.488+66T>A
ENST00000674845.1:c.*854+66T>A ENSP00000502309.1:n.*854+66T>A
ENST00000674856.1:n.147-6327T>A
ENST00000675147.1:c.327+66T>A ENSP00000501840.1:n.327+66T>A
ENST00000675221.1:c.273+66T>A ENSP00000502761.1:n.273+66T>A
ENST00000675434.1:n.212+66T>A
ENST00000675502.1:c.-16+66T>A ENSP00000502428.1:n.-16+66T>A
ENST00000675801.1:c.-16+66T>A ENSP00000502688.1:n.-16+66T>A
ENST00000675865.1:c.-16+66T>A ENSP00000502003.1:n.-16+66T>A
ENST00000676024.1:c.348+66T>A ENSP00000502105.1:n.348+66T>A
ENST00000676223.1:c.309+66T>A ENSP00000502361.1:n.309+66T>A
ENST00000676226.1:c.-16+66T>A ENSP00000502325.1:n.-16+66T>A
ENST00000676251.1:n.530+66T>A
ENST00000256830.13:c.348+66T>A ENSP00000256830.8:n.348+66T>A
ENST00000356462.10:c.348+66T>A ENSP00000348847.5:n.348+66T>A
ENST00000357895.9:c.324+66T>A ENSP00000350569.4:n.324+66T>A
ENST00000382850.8:c.348+66T>A ENSP00000372301.3:n.348+66T>A
ENST00000400345.7:c.348+66T>A ENSP00000383199.2:n.348+66T>A
ENST00000431212.6:c.-16+66T>A ENSP00000389406.1:n.-16+66T>A
ENST00000435432.6:c.-16+66T>A ENSP00000393395.1:n.-16+66T>A
ENST00000456173.6:c.-16+66T>A ENSP00000405440.1:n.-16+66T>A
ENST00000456986.5:c.-16+66T>A ENSP00000411947.1:n.-16+66T>A
ENST00000586263.5:c.324+66T>A ENSP00000468546.1:n.324+66T>A
ENST00000586268.5:c.-15-6327T>A ENSP00000467072.1:n.-15-6327T>A
ENST00000587190.5:c.-16+66T>A ENSP00000467768.1:n.-16+66T>A
ENST00000587634.5:n.488+66T>A
ENST00000588066.5:n.327+66T>A
ENST00000588494.5:c.-16+66T>A ENSP00000466789.1:n.-16+66T>A
ENST00000589054.5:c.49-74548T>A ENSP00000465669.1:n.49-74548T>A
ENST00000592601.5:n.86+66T>A
ENST00000592846.5:c.-16+66T>A ENSP00000466776.1:n.-16+66T>A
NM_001144964.1:c.-16+66T>A NP_001138436.1:n.-16+66T>A
NM_001144965.1:c.-16+66T>A NP_001138437.1:n.-16+66T>A
NM_001144966.2:c.-16+66T>A NP_001138438.1:n.-16+66T>A
NM_001144967.2:c.348+66T>A NP_001138439.1:n.348+66T>A
NM_001144968.1:c.324+66T>A NP_001138440.1:n.324+66T>A
NM_001144969.1:c.324+66T>A NP_001138441.1:n.324+66T>A
NM_001144970.2:c.-16+66T>A NP_001138442.1:n.-16+66T>A
NM_001144971.1:c.-16+66T>A NP_001138443.1:n.-16+66T>A
NM_001243960.1:c.348+66T>A NP_001230889.1:n.348+66T>A
NM_015277.5:c.348+66T>A NP_056092.2:n.348+66T>A
XM_005266658.3:c.249+66T>A XP_005266715.2:n.249+66T>A
XM_005266660.3:c.249+66T>A XP_005266717.2:n.249+66T>A
XM_005266663.3:c.249+66T>A XP_005266720.2:n.249+66T>A
XM_006722421.2:c.249+66T>A XP_006722484.2:n.249+66T>A
XM_006722424.2:c.249+66T>A XP_006722487.2:n.249+66T>A
XM_006722425.2:c.249+66T>A XP_006722488.2:n.249+66T>A
XM_006722426.2:c.426+66T>A XP_006722489.1:n.426+66T>A
XM_006722428.2:c.348+66T>A XP_006722491.1:n.348+66T>A
XM_006722430.2:c.-16+66T>A XP_006722493.1:n.-16+66T>A
XM_011525887.1:c.402+66T>A XP_011524189.1:n.402+66T>A
XM_005266658.4:c.249+66T>A XP_005266715.2:n.249+66T>A
XM_005266660.4:c.249+66T>A XP_005266717.2:n.249+66T>A
XM_005266663.4:c.249+66T>A XP_005266720.2:n.249+66T>A
XM_006722421.4:c.249+66T>A XP_006722484.2:n.249+66T>A
XM_006722424.3:c.249+66T>A XP_006722487.2:n.249+66T>A
XM_006722425.3:c.249+66T>A XP_006722488.2:n.249+66T>A
XM_006722426.4:c.426+66T>A XP_006722489.1:n.426+66T>A
XM_006722428.4:c.348+66T>A XP_006722491.1:n.348+66T>A
XM_006722430.4:c.-16+66T>A XP_006722493.1:n.-16+66T>A
XM_011525887.3:c.402+66T>A XP_011524189.1:n.402+66T>A
XM_017025676.1:c.249+66T>A XP_016881165.1:n.249+66T>A
XM_017025677.1:c.249+66T>A XP_016881166.1:n.249+66T>A
XM_017025678.2:c.348+66T>A XP_016881167.1:n.348+66T>A
XM_017025679.2:c.-16+66T>A XP_016881168.1:n.-16+66T>A
XM_017025680.2:c.-16+66T>A XP_016881169.1:n.-16+66T>A
XM_017025681.2:c.-16+66T>A XP_016881170.1:n.-16+66T>A
XM_024451129.1:c.-16+66T>A XP_024306897.1:n.-16+66T>A
XM_024451130.1:c.-16+66T>A XP_024306898.1:n.-16+66T>A
XM_024451131.1:c.-16+66T>A XP_024306899.1:n.-16+66T>A
XM_024451132.1:c.-16+66T>A XP_024306900.1:n.-16+66T>A
XM_024451133.1:c.-16+66T>A XP_024306901.1:n.-16+66T>A
XM_024451134.1:c.-16+66T>A XP_024306902.1:n.-16+66T>A
XM_024451135.1:c.-16+66T>A XP_024306903.1:n.-16+66T>A
XM_024451136.1:c.-16+66T>A XP_024306904.1:n.-16+66T>A
XM_024451137.1:c.-16+66T>A XP_024306905.1:n.-16+66T>A
NM_001144967.3:c.348+66T>A MANE Select NP_001138439.1:n.348+66T>A
NM_001144965.2:c.-16+66T>A NP_001138437.1:n.-16+66T>A
NM_001144966.3:c.-16+66T>A NP_001138438.1:n.-16+66T>A
NM_001144968.2:c.324+66T>A NP_001138440.1:n.324+66T>A
NM_001144969.2:c.324+66T>A NP_001138441.1:n.324+66T>A
NM_001144970.3:c.-16+66T>A NP_001138442.1:n.-16+66T>A
NM_001144971.2:c.-16+66T>A NP_001138443.1:n.-16+66T>A
NM_001243960.2:c.348+66T>A NP_001230889.1:n.348+66T>A
NM_015277.6:c.348+66T>A NP_056092.2:n.348+66T>A
Search 100 bp 5'
Search 100 bp 3'