Canonical Allele Identifier: CA2641962355

Gene: NEDD4L

Linked Data

• gnomAD v4: 18-58165951-ACTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58165955_58165957del , CM000680.2:g.58165955_58165957del	GRCh38
NC_000018.9:g.55833187_55833189del , CM000680.1:g.55833187_55833189del	GRCh37
NC_000018.8:g.53984185_53984187del	NCBI36
NG_029954.1:g.126578_126580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400345.8:c.122+94_122+96del MANE Select	ENSP00000383199.2:n.122+94_122+96del
ENST00000585594.6:n.193_195del
ENST00000674613.1:n.98-79472_98-79470del
ENST00000674845.1:c.*628+94_*628+96del	ENSP00000502309.1:n.*628+94_*628+96del
ENST00000675137.1:n.244+94_244+96del
ENST00000675147.1:c.101+94_101+96del	ENSP00000501840.1:n.101+94_101+96del
ENST00000675502.1:c.-242+94_-242+96del	ENSP00000502428.1:n.-242+94_-242+96del
ENST00000675801.1:c.-242+94_-242+96del	ENSP00000502688.1:n.-242+94_-242+96del
ENST00000676024.1:c.122+94_122+96del	ENSP00000502105.1:n.122+94_122+96del
ENST00000676223.1:c.83+94_83+96del	ENSP00000502361.1:n.83+94_83+96del
ENST00000256830.13:c.122+94_122+96del	ENSP00000256830.8:n.122+94_122+96del
ENST00000356462.10:c.122+94_122+96del	ENSP00000348847.5:n.122+94_122+96del
ENST00000357895.9:c.98+94_98+96del	ENSP00000350569.4:n.98+94_98+96del
ENST00000382850.8:c.122+94_122+96del	ENSP00000372301.3:n.122+94_122+96del
ENST00000400345.7:c.122+94_122+96del	ENSP00000383199.2:n.122+94_122+96del
ENST00000435432.6:c.-320+94_-320+96del	ENSP00000393395.1:n.-320+94_-320+96del
ENST00000456986.5:c.-242+94_-242+96del	ENSP00000411947.1:n.-242+94_-242+96del
ENST00000585363.5:n.159+94_159+96del
ENST00000586263.5:c.98+94_98+96del	ENSP00000468546.1:n.98+94_98+96del
ENST00000588516.5:n.1222+94_1222+96del
ENST00000589054.5:c.48+121247_48+121249del	ENSP00000465669.1:n.48+121247_48+121249del
ENST00000591989.5:n.170+94_170+96del
ENST00000592846.5:c.-301+94_-301+96del	ENSP00000466776.1:n.-301+94_-301+96del
NM_001144964.1:c.-242+94_-242+96del	NP_001138436.1:n.-242+94_-242+96del
NM_001144965.1:c.-242+94_-242+96del	NP_001138437.1:n.-242+94_-242+96del
NM_001144967.2:c.122+94_122+96del	NP_001138439.1:n.122+94_122+96del
NM_001144968.1:c.98+94_98+96del	NP_001138440.1:n.98+94_98+96del
NM_001144969.1:c.98+94_98+96del	NP_001138441.1:n.98+94_98+96del
NM_001144971.1:c.-320+94_-320+96del	NP_001138443.1:n.-320+94_-320+96del
NM_001243960.1:c.122+94_122+96del	NP_001230889.1:n.122+94_122+96del
NM_015277.5:c.122+94_122+96del	NP_056092.2:n.122+94_122+96del
XM_006722426.2:c.122+94_122+96del	XP_006722489.1:n.122+94_122+96del
XM_006722428.2:c.122+94_122+96del	XP_006722491.1:n.122+94_122+96del
XM_011525887.1:c.98+94_98+96del	XP_011524189.1:n.98+94_98+96del
XM_006722426.4:c.122+94_122+96del	XP_006722489.1:n.122+94_122+96del
XM_006722428.4:c.122+94_122+96del	XP_006722491.1:n.122+94_122+96del
XM_011525887.3:c.98+94_98+96del	XP_011524189.1:n.98+94_98+96del
XM_017025678.2:c.122+94_122+96del	XP_016881167.1:n.122+94_122+96del
XM_024451129.1:c.-320+94_-320+96del	XP_024306897.1:n.-320+94_-320+96del
XM_024451131.1:c.-242+94_-242+96del	XP_024306899.1:n.-242+94_-242+96del
XM_024451134.1:c.-301+94_-301+96del	XP_024306902.1:n.-301+94_-301+96del
XM_024451135.1:c.-242+94_-242+96del	XP_024306903.1:n.-242+94_-242+96del
XM_024451136.1:c.-242+94_-242+96del	XP_024306904.1:n.-242+94_-242+96del
XM_024451137.1:c.-320+94_-320+96del	XP_024306905.1:n.-320+94_-320+96del
NM_001144967.3:c.122+94_122+96del MANE Select	NP_001138439.1:n.122+94_122+96del
NM_001144965.2:c.-242+94_-242+96del	NP_001138437.1:n.-242+94_-242+96del
NM_001144968.2:c.98+94_98+96del	NP_001138440.1:n.98+94_98+96del
NM_001144969.2:c.98+94_98+96del	NP_001138441.1:n.98+94_98+96del
NM_001144971.2:c.-320+94_-320+96del	NP_001138443.1:n.-320+94_-320+96del
NM_001243960.2:c.122+94_122+96del	NP_001230889.1:n.122+94_122+96del
NM_015277.6:c.122+94_122+96del	NP_056092.2:n.122+94_122+96del