Canonical Allele Identifier: CA402715254
Gene: NEDD4L HGNC NCBI

Linked Data

dbSNP Id: rs1248936515

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58165815G>A , CM000680.2:g.58165815G>A GRCh38
NC_000018.9:g.55833047G>A , CM000680.1:g.55833047G>A GRCh37
NC_000018.8:g.53984045G>A NCBI36
NG_029954.1:g.126438G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400345.8:c.76G>A MANE Select ENSP00000383199.2:p.Val26Ile
ENST00000585594.6:n.53G>A
ENST00000674613.1:n.98-79612G>A
ENST00000674845.1:c.*582G>A ENSP00000502309.1:n.*582G>A
ENST00000675137.1:n.198G>A
ENST00000675147.1:c.55G>A ENSP00000501840.1:p.Val19Ile
ENST00000675502.1:c.-288G>A ENSP00000502428.1:n.-288G>A
ENST00000675801.1:c.-288G>A ENSP00000502688.1:n.-288G>A
ENST00000676024.1:c.76G>A ENSP00000502105.1:p.Val26Ile
ENST00000676223.1:c.37G>A ENSP00000502361.1:p.Val13Ile
ENST00000256830.13:c.76G>A ENSP00000256830.8:p.Val26Ile
ENST00000356462.10:c.76G>A ENSP00000348847.5:p.Val26Ile
ENST00000357895.9:c.52G>A ENSP00000350569.4:p.Val18Ile
ENST00000382850.8:c.76G>A ENSP00000372301.3:p.Val26Ile
ENST00000400345.7:c.76G>A ENSP00000383199.2:p.Val26Ile
ENST00000435432.6:c.-366G>A ENSP00000393395.1:n.-366G>A
ENST00000456986.5:c.-288G>A ENSP00000411947.1:n.-288G>A
ENST00000585363.5:n.113G>A
ENST00000585594.5:n.196G>A
ENST00000586263.5:c.52G>A ENSP00000468546.1:p.Val18Ile
ENST00000587547.1:n.865G>A
ENST00000588516.5:n.1176G>A
ENST00000589054.5:c.48+121107G>A ENSP00000465669.1:n.48+121107G>A
ENST00000590694.5:n.119G>A
ENST00000591579.5:n.120G>A
ENST00000591989.5:n.124G>A
ENST00000592846.5:c.-347G>A ENSP00000466776.1:n.-347G>A
NM_001144964.1:c.-288G>A NP_001138436.1:n.-288G>A
NM_001144965.1:c.-288G>A NP_001138437.1:n.-288G>A
NM_001144967.2:c.76G>A NP_001138439.1:p.Val26Ile
NM_001144968.1:c.52G>A NP_001138440.1:p.Val18Ile
NM_001144969.1:c.52G>A NP_001138441.1:p.Val18Ile
NM_001144971.1:c.-366G>A NP_001138443.1:n.-366G>A
NM_001243960.1:c.76G>A NP_001230889.1:p.Val26Ile
NM_015277.5:c.76G>A NP_056092.2:p.Val26Ile
XM_006722426.2:c.76G>A XP_006722489.1:p.Val26Ile
XM_006722428.2:c.76G>A XP_006722491.1:p.Val26Ile
XM_011525887.1:c.52G>A XP_011524189.1:p.Val18Ile
XM_006722426.4:c.76G>A XP_006722489.1:p.Val26Ile
XM_006722428.4:c.76G>A XP_006722491.1:p.Val26Ile
XM_011525887.3:c.52G>A XP_011524189.1:p.Val18Ile
XM_017025678.2:c.76G>A XP_016881167.1:p.Val26Ile
XM_024451129.1:c.-366G>A XP_024306897.1:n.-366G>A
XM_024451131.1:c.-288G>A XP_024306899.1:n.-288G>A
XM_024451134.1:c.-347G>A XP_024306902.1:n.-347G>A
XM_024451135.1:c.-288G>A XP_024306903.1:n.-288G>A
XM_024451136.1:c.-288G>A XP_024306904.1:n.-288G>A
XM_024451137.1:c.-366G>A XP_024306905.1:n.-366G>A
NM_001144967.3:c.76G>A MANE Select NP_001138439.1:p.Val26Ile
NM_001144965.2:c.-288G>A NP_001138437.1:n.-288G>A
NM_001144968.2:c.52G>A NP_001138440.1:p.Val18Ile
NM_001144969.2:c.52G>A NP_001138441.1:p.Val18Ile
NM_001144971.2:c.-366G>A NP_001138443.1:n.-366G>A
NM_001243960.2:c.76G>A NP_001230889.1:p.Val26Ile
NM_015277.6:c.76G>A NP_056092.2:p.Val26Ile