Canonical Allele Identifier: CA2641962255

Gene: NEDD4L

Linked Data

• gnomAD v4: 18-58165696-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58165697_58165698del , CM000680.2:g.58165697_58165698del	GRCh38
NC_000018.9:g.55832929_55832930del , CM000680.1:g.55832929_55832930del	GRCh37
NC_000018.8:g.53983927_53983928del	NCBI36
NG_029954.1:g.126320_126321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400345.8:c.49-91_49-90del MANE Select	ENSP00000383199.2:n.49-91_49-90del
ENST00000585594.6:n.26-91_26-90del
ENST00000674613.1:n.98-79730_98-79729del
ENST00000674845.1:c.*555-91_*555-90del	ENSP00000502309.1:n.*555-91_*555-90del
ENST00000675137.1:n.171-91_171-90del
ENST00000675147.1:c.28-91_28-90del	ENSP00000501840.1:n.28-91_28-90del
ENST00000675227.1:c.95-91_95-90del	ENSP00000502649.1:n.95-91_95-90del
ENST00000675502.1:c.-315-91_-315-90del	ENSP00000502428.1:n.-315-91_-315-90del
ENST00000675554.1:n.165-91_165-90del
ENST00000675801.1:c.-315-91_-315-90del	ENSP00000502688.1:n.-315-91_-315-90del
ENST00000676024.1:c.49-91_49-90del	ENSP00000502105.1:n.49-91_49-90del
ENST00000676223.1:c.10-91_10-90del	ENSP00000502361.1:n.10-91_10-90del
ENST00000256830.13:c.49-91_49-90del	ENSP00000256830.8:n.49-91_49-90del
ENST00000356462.10:c.49-91_49-90del	ENSP00000348847.5:n.49-91_49-90del
ENST00000357895.9:c.25-91_25-90del	ENSP00000350569.4:n.25-91_25-90del
ENST00000382850.8:c.49-91_49-90del	ENSP00000372301.3:n.49-91_49-90del
ENST00000400345.7:c.49-91_49-90del	ENSP00000383199.2:n.49-91_49-90del
ENST00000435432.6:c.-393-91_-393-90del	ENSP00000393395.1:n.-393-91_-393-90del
ENST00000456986.5:c.-315-91_-315-90del	ENSP00000411947.1:n.-315-91_-315-90del
ENST00000585363.5:n.86-91_86-90del
ENST00000585594.5:n.169-91_169-90del
ENST00000586263.5:c.25-91_25-90del	ENSP00000468546.1:n.25-91_25-90del
ENST00000587547.1:n.838-91_838-90del
ENST00000588516.5:n.1149-91_1149-90del
ENST00000589054.5:c.48+120989_48+120990del	ENSP00000465669.1:n.48+120989_48+120990del
ENST00000590694.5:n.92-91_92-90del
ENST00000591579.5:n.93-91_93-90del
ENST00000591989.5:n.101-95_101-94del
ENST00000592846.5:c.-370-95_-370-94del	ENSP00000466776.1:n.-370-95_-370-94del
NM_001144964.1:c.-315-91_-315-90del	NP_001138436.1:n.-315-91_-315-90del
NM_001144965.1:c.-315-91_-315-90del	NP_001138437.1:n.-315-91_-315-90del
NM_001144967.2:c.49-91_49-90del	NP_001138439.1:n.49-91_49-90del
NM_001144968.1:c.25-91_25-90del	NP_001138440.1:n.25-91_25-90del
NM_001144969.1:c.25-91_25-90del	NP_001138441.1:n.25-91_25-90del
NM_001144971.1:c.-393-91_-393-90del	NP_001138443.1:n.-393-91_-393-90del
NM_001243960.1:c.49-91_49-90del	NP_001230889.1:n.49-91_49-90del
NM_015277.5:c.49-91_49-90del	NP_056092.2:n.49-91_49-90del
XM_006722426.2:c.49-91_49-90del	XP_006722489.1:n.49-91_49-90del
XM_006722428.2:c.49-91_49-90del	XP_006722491.1:n.49-91_49-90del
XM_011525887.1:c.25-91_25-90del	XP_011524189.1:n.25-91_25-90del
XM_006722426.4:c.49-91_49-90del	XP_006722489.1:n.49-91_49-90del
XM_006722428.4:c.49-91_49-90del	XP_006722491.1:n.49-91_49-90del
XM_011525887.3:c.25-91_25-90del	XP_011524189.1:n.25-91_25-90del
XM_017025678.2:c.49-91_49-90del	XP_016881167.1:n.49-91_49-90del
XM_024451129.1:c.-393-91_-393-90del	XP_024306897.1:n.-393-91_-393-90del
XM_024451131.1:c.-315-91_-315-90del	XP_024306899.1:n.-315-91_-315-90del
XM_024451134.1:c.-374-91_-374-90del	XP_024306902.1:n.-374-91_-374-90del
XM_024451135.1:c.-315-91_-315-90del	XP_024306903.1:n.-315-91_-315-90del
XM_024451136.1:c.-315-91_-315-90del	XP_024306904.1:n.-315-91_-315-90del
XM_024451137.1:c.-393-91_-393-90del	XP_024306905.1:n.-393-91_-393-90del
NM_001144967.3:c.49-91_49-90del MANE Select	NP_001138439.1:n.49-91_49-90del
NM_001144965.2:c.-315-91_-315-90del	NP_001138437.1:n.-315-91_-315-90del
NM_001144968.2:c.25-91_25-90del	NP_001138440.1:n.25-91_25-90del
NM_001144969.2:c.25-91_25-90del	NP_001138441.1:n.25-91_25-90del
NM_001144971.2:c.-393-91_-393-90del	NP_001138443.1:n.-393-91_-393-90del
NM_001243960.2:c.49-91_49-90del	NP_001230889.1:n.49-91_49-90del
NM_015277.6:c.49-91_49-90del	NP_056092.2:n.49-91_49-90del