Canonical Allele Identifier: CA2641962291

Gene: NEDD4L

Linked Data

• gnomAD v4: 18-58165761-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58165764_58165765dup , CM000680.2:g.58165764_58165765dup	GRCh38
NC_000018.9:g.55832996_55832997dup , CM000680.1:g.55832996_55832997dup	GRCh37
NC_000018.8:g.53983994_53983995dup	NCBI36
NG_029954.1:g.126387_126388dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400345.8:c.49-24_49-23dup MANE Select	ENSP00000383199.2:n.49-24_49-23dup
ENST00000585594.6:n.26-24_26-23dup
ENST00000674613.1:n.98-79663_98-79662dup
ENST00000674845.1:c.*555-24_*555-23dup	ENSP00000502309.1:n.*555-24_*555-23dup
ENST00000675137.1:n.171-24_171-23dup
ENST00000675147.1:c.28-24_28-23dup	ENSP00000501840.1:n.28-24_28-23dup
ENST00000675227.1:c.95-24_95-23dup	ENSP00000502649.1:n.95-24_95-23dup
ENST00000675502.1:c.-315-24_-315-23dup	ENSP00000502428.1:n.-315-24_-315-23dup
ENST00000675554.1:n.165-24_165-23dup
ENST00000675801.1:c.-315-24_-315-23dup	ENSP00000502688.1:n.-315-24_-315-23dup
ENST00000676024.1:c.49-24_49-23dup	ENSP00000502105.1:n.49-24_49-23dup
ENST00000676223.1:c.10-24_10-23dup	ENSP00000502361.1:n.10-24_10-23dup
ENST00000256830.13:c.49-24_49-23dup	ENSP00000256830.8:n.49-24_49-23dup
ENST00000356462.10:c.49-24_49-23dup	ENSP00000348847.5:n.49-24_49-23dup
ENST00000357895.9:c.25-24_25-23dup	ENSP00000350569.4:n.25-24_25-23dup
ENST00000382850.8:c.49-24_49-23dup	ENSP00000372301.3:n.49-24_49-23dup
ENST00000400345.7:c.49-24_49-23dup	ENSP00000383199.2:n.49-24_49-23dup
ENST00000435432.6:c.-393-24_-393-23dup	ENSP00000393395.1:n.-393-24_-393-23dup
ENST00000456986.5:c.-315-24_-315-23dup	ENSP00000411947.1:n.-315-24_-315-23dup
ENST00000585363.5:n.86-24_86-23dup
ENST00000585594.5:n.169-24_169-23dup
ENST00000586263.5:c.25-24_25-23dup	ENSP00000468546.1:n.25-24_25-23dup
ENST00000587547.1:n.838-24_838-23dup
ENST00000588516.5:n.1149-24_1149-23dup
ENST00000589054.5:c.48+121056_48+121057dup	ENSP00000465669.1:n.48+121056_48+121057dup
ENST00000590694.5:n.92-24_92-23dup
ENST00000591579.5:n.93-24_93-23dup
ENST00000591989.5:n.101-28_101-27dup
ENST00000592846.5:c.-370-28_-370-27dup	ENSP00000466776.1:n.-370-28_-370-27dup
NM_001144964.1:c.-315-24_-315-23dup	NP_001138436.1:n.-315-24_-315-23dup
NM_001144965.1:c.-315-24_-315-23dup	NP_001138437.1:n.-315-24_-315-23dup
NM_001144967.2:c.49-24_49-23dup	NP_001138439.1:n.49-24_49-23dup
NM_001144968.1:c.25-24_25-23dup	NP_001138440.1:n.25-24_25-23dup
NM_001144969.1:c.25-24_25-23dup	NP_001138441.1:n.25-24_25-23dup
NM_001144971.1:c.-393-24_-393-23dup	NP_001138443.1:n.-393-24_-393-23dup
NM_001243960.1:c.49-24_49-23dup	NP_001230889.1:n.49-24_49-23dup
NM_015277.5:c.49-24_49-23dup	NP_056092.2:n.49-24_49-23dup
XM_006722426.2:c.49-24_49-23dup	XP_006722489.1:n.49-24_49-23dup
XM_006722428.2:c.49-24_49-23dup	XP_006722491.1:n.49-24_49-23dup
XM_011525887.1:c.25-24_25-23dup	XP_011524189.1:n.25-24_25-23dup
XM_006722426.4:c.49-24_49-23dup	XP_006722489.1:n.49-24_49-23dup
XM_006722428.4:c.49-24_49-23dup	XP_006722491.1:n.49-24_49-23dup
XM_011525887.3:c.25-24_25-23dup	XP_011524189.1:n.25-24_25-23dup
XM_017025678.2:c.49-24_49-23dup	XP_016881167.1:n.49-24_49-23dup
XM_024451129.1:c.-393-24_-393-23dup	XP_024306897.1:n.-393-24_-393-23dup
XM_024451131.1:c.-315-24_-315-23dup	XP_024306899.1:n.-315-24_-315-23dup
XM_024451134.1:c.-374-24_-374-23dup	XP_024306902.1:n.-374-24_-374-23dup
XM_024451135.1:c.-315-24_-315-23dup	XP_024306903.1:n.-315-24_-315-23dup
XM_024451136.1:c.-315-24_-315-23dup	XP_024306904.1:n.-315-24_-315-23dup
XM_024451137.1:c.-393-24_-393-23dup	XP_024306905.1:n.-393-24_-393-23dup
NM_001144967.3:c.49-24_49-23dup MANE Select	NP_001138439.1:n.49-24_49-23dup
NM_001144965.2:c.-315-24_-315-23dup	NP_001138437.1:n.-315-24_-315-23dup
NM_001144968.2:c.25-24_25-23dup	NP_001138440.1:n.25-24_25-23dup
NM_001144969.2:c.25-24_25-23dup	NP_001138441.1:n.25-24_25-23dup
NM_001144971.2:c.-393-24_-393-23dup	NP_001138443.1:n.-393-24_-393-23dup
NM_001243960.2:c.49-24_49-23dup	NP_001230889.1:n.49-24_49-23dup
NM_015277.6:c.49-24_49-23dup	NP_056092.2:n.49-24_49-23dup