Canonical Allele Identifier: CA2306329133
Gene: NEDD4L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58165828T= , CM000680.2:g.58165828T= GRCh38
NC_000018.9:g.55833060T= , CM000680.1:g.55833060T= GRCh37
NC_000018.8:g.53984058T= NCBI36
NG_029954.1:g.126451T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400345.8:c.89T= MANE Select ENSP00000383199.2:p.Ile30=
ENST00000585594.6:n.66T=
ENST00000674613.1:n.98-79599T=
ENST00000674845.1:c.*595T= ENSP00000502309.1:n.*595T=
ENST00000675137.1:n.211T=
ENST00000675147.1:c.68T= ENSP00000501840.1:p.Ile23=
ENST00000675502.1:c.-275T= ENSP00000502428.1:n.-275T=
ENST00000675801.1:c.-275T= ENSP00000502688.1:n.-275T=
ENST00000676024.1:c.89T= ENSP00000502105.1:p.Ile30=
ENST00000676223.1:c.50T= ENSP00000502361.1:p.Ile17=
ENST00000256830.13:c.89T= ENSP00000256830.8:p.Ile30=
ENST00000356462.10:c.89T= ENSP00000348847.5:p.Ile30=
ENST00000357895.9:c.65T= ENSP00000350569.4:p.Ile22=
ENST00000382850.8:c.89T= ENSP00000372301.3:p.Ile30=
ENST00000400345.7:c.89T= ENSP00000383199.2:p.Ile30=
ENST00000435432.6:c.-353T= ENSP00000393395.1:n.-353T=
ENST00000456986.5:c.-275T= ENSP00000411947.1:n.-275T=
ENST00000585363.5:n.126T=
ENST00000585594.5:n.209T=
ENST00000586263.5:c.65T= ENSP00000468546.1:p.Ile22=
ENST00000587547.1:n.878T=
ENST00000588516.5:n.1189T=
ENST00000589054.5:c.48+121120T= ENSP00000465669.1:n.48+121120T=
ENST00000590694.5:n.132T=
ENST00000591579.5:n.133T=
ENST00000591989.5:n.137T=
ENST00000592846.5:c.-334T= ENSP00000466776.1:n.-334T=
NM_001144964.1:c.-275T= NP_001138436.1:n.-275T=
NM_001144965.1:c.-275T= NP_001138437.1:n.-275T=
NM_001144967.2:c.89T= NP_001138439.1:p.Ile30=
NM_001144968.1:c.65T= NP_001138440.1:p.Ile22=
NM_001144969.1:c.65T= NP_001138441.1:p.Ile22=
NM_001144971.1:c.-353T= NP_001138443.1:n.-353T=
NM_001243960.1:c.89T= NP_001230889.1:p.Ile30=
NM_015277.5:c.89T= NP_056092.2:p.Ile30=
XM_006722426.2:c.89T= XP_006722489.1:p.Ile30=
XM_006722428.2:c.89T= XP_006722491.1:p.Ile30=
XM_011525887.1:c.65T= XP_011524189.1:p.Ile22=
XM_006722426.4:c.89T= XP_006722489.1:p.Ile30=
XM_006722428.4:c.89T= XP_006722491.1:p.Ile30=
XM_011525887.3:c.65T= XP_011524189.1:p.Ile22=
XM_017025678.2:c.89T= XP_016881167.1:p.Ile30=
XM_024451129.1:c.-353T= XP_024306897.1:n.-353T=
XM_024451131.1:c.-275T= XP_024306899.1:n.-275T=
XM_024451134.1:c.-334T= XP_024306902.1:n.-334T=
XM_024451135.1:c.-275T= XP_024306903.1:n.-275T=
XM_024451136.1:c.-275T= XP_024306904.1:n.-275T=
XM_024451137.1:c.-353T= XP_024306905.1:n.-353T=
NM_001144967.3:c.89T= MANE Select NP_001138439.1:p.Ile30=
NM_001144965.2:c.-275T= NP_001138437.1:n.-275T=
NM_001144968.2:c.65T= NP_001138440.1:p.Ile22=
NM_001144969.2:c.65T= NP_001138441.1:p.Ile22=
NM_001144971.2:c.-353T= NP_001138443.1:n.-353T=
NM_001243960.2:c.89T= NP_001230889.1:p.Ile30=
NM_015277.6:c.89T= NP_056092.2:p.Ile30=