Canonical Allele Identifier: CA2735325977

Gene: NEDD4L

Linked Data

• dbSNP Id: rs2146272802

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58149293_58149297dup , CM000680.2:g.58149293_58149297dup	GRCh38
NC_000018.9:g.55816525_55816529dup , CM000680.1:g.55816525_55816529dup	GRCh37
NC_000018.8:g.53967523_53967527dup	NCBI36
NG_029954.1:g.109916_109920dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000400345.8:c.49-16495_49-16491dup MANE Select	ENSP00000383199.2:n.49-16495_49-16491dup
ENST00000585594.6:n.26-16495_26-16491dup
ENST00000674613.1:n.98-96134_98-96130dup
ENST00000674845.1:c.*555-16495_*555-16491dup	ENSP00000502309.1:n.*555-16495_*555-16491dup
ENST00000675137.1:n.171-16495_171-16491dup
ENST00000675147.1:c.28-16495_28-16491dup	ENSP00000501840.1:n.28-16495_28-16491dup
ENST00000675227.1:c.95-16495_95-16491dup	ENSP00000502649.1:n.95-16495_95-16491dup
ENST00000675502.1:c.-315-16495_-315-16491dup	ENSP00000502428.1:n.-315-16495_-315-16491dup
ENST00000675554.1:n.165-16495_165-16491dup
ENST00000675801.1:c.-315-16495_-315-16491dup	ENSP00000502688.1:n.-315-16495_-315-16491dup
ENST00000676024.1:c.49-16495_49-16491dup	ENSP00000502105.1:n.49-16495_49-16491dup
ENST00000676223.1:c.10-16495_10-16491dup	ENSP00000502361.1:n.10-16495_10-16491dup
ENST00000256830.13:c.49-16495_49-16491dup	ENSP00000256830.8:n.49-16495_49-16491dup
ENST00000356462.10:c.49-16495_49-16491dup	ENSP00000348847.5:n.49-16495_49-16491dup
ENST00000382850.8:c.49-16495_49-16491dup	ENSP00000372301.3:n.49-16495_49-16491dup
ENST00000400345.7:c.49-16495_49-16491dup	ENSP00000383199.2:n.49-16495_49-16491dup
ENST00000456986.5:c.-315-16495_-315-16491dup	ENSP00000411947.1:n.-315-16495_-315-16491dup
ENST00000585363.5:n.86-16495_86-16491dup
ENST00000585594.5:n.169-16495_169-16491dup
ENST00000587547.1:n.838-16495_838-16491dup
ENST00000588516.5:n.1149-16495_1149-16491dup
ENST00000589054.5:c.48+104585_48+104589dup	ENSP00000465669.1:n.48+104585_48+104589dup
ENST00000590694.5:n.92-16495_92-16491dup
ENST00000591579.5:n.93-16495_93-16491dup
ENST00000591989.5:n.101-16499_101-16495dup
ENST00000592846.5:c.-370-16499_-370-16495dup	ENSP00000466776.1:n.-370-16499_-370-16495dup
NM_001144964.1:c.-315-16495_-315-16491dup	NP_001138436.1:n.-315-16495_-315-16491dup
NM_001144967.2:c.49-16495_49-16491dup	NP_001138439.1:n.49-16495_49-16491dup
NM_001243960.1:c.49-16495_49-16491dup	NP_001230889.1:n.49-16495_49-16491dup
NM_015277.5:c.49-16495_49-16491dup	NP_056092.2:n.49-16495_49-16491dup
XM_006722426.2:c.49-16495_49-16491dup	XP_006722489.1:n.49-16495_49-16491dup
XM_006722428.2:c.49-16495_49-16491dup	XP_006722491.1:n.49-16495_49-16491dup
XM_011525887.1:c.-243_-239dup	XP_011524189.1:n.-243_-239dup
XM_006722426.4:c.49-16495_49-16491dup	XP_006722489.1:n.49-16495_49-16491dup
XM_006722428.4:c.49-16495_49-16491dup	XP_006722491.1:n.49-16495_49-16491dup
XM_011525887.3:c.-243_-239dup	XP_011524189.1:n.-243_-239dup
XM_017025678.2:c.49-16495_49-16491dup	XP_016881167.1:n.49-16495_49-16491dup
XM_024451129.1:c.-393-16495_-393-16491dup	XP_024306897.1:n.-393-16495_-393-16491dup
XM_024451131.1:c.-315-16495_-315-16491dup	XP_024306899.1:n.-315-16495_-315-16491dup
XM_024451134.1:c.-651_-647dup	XP_024306902.1:n.-651_-647dup
XM_024451135.1:c.-315-16495_-315-16491dup	XP_024306903.1:n.-315-16495_-315-16491dup
XM_024451136.1:c.-315-16495_-315-16491dup	XP_024306904.1:n.-315-16495_-315-16491dup
XM_024451137.1:c.-393-16495_-393-16491dup	XP_024306905.1:n.-393-16495_-393-16491dup
NM_001144967.3:c.49-16495_49-16491dup MANE Select	NP_001138439.1:n.49-16495_49-16491dup
NM_001243960.2:c.49-16495_49-16491dup	NP_001230889.1:n.49-16495_49-16491dup
NM_015277.6:c.49-16495_49-16491dup	NP_056092.2:n.49-16495_49-16491dup