Canonical Allele Identifier: CA2306329132

Gene: NEDD4L

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58165823_58165825delinsTGG , CM000680.2:g.58165823_58165825delinsTGG	GRCh38
NC_000018.9:g.55833055_55833057delinsTGG , CM000680.1:g.55833055_55833057delinsTGG	GRCh37
NC_000018.8:g.53984053_53984055delinsTGG	NCBI36
NG_029954.1:g.126446_126448delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400345.8:c.84_86delinsTGG MANE Select	ENSP00000383199.2:p.Ser28=
ENST00000585594.6:n.61_63delinsTGG
ENST00000674613.1:n.98-79604_98-79602delinsTGG
ENST00000674845.1:c.*590_*592delinsTGG	ENSP00000502309.1:n.*590_*592delinsTGG
ENST00000675137.1:n.206_208delinsTGG
ENST00000675147.1:c.63_65delinsTGG	ENSP00000501840.1:p.Ser21=
ENST00000675502.1:c.-280_-278delinsTGG	ENSP00000502428.1:n.-280_-278delinsTGG
ENST00000675801.1:c.-280_-278delinsTGG	ENSP00000502688.1:n.-280_-278delinsTGG
ENST00000676024.1:c.84_86delinsTGG	ENSP00000502105.1:p.Ser28=
ENST00000676223.1:c.45_47delinsTGG	ENSP00000502361.1:p.Ser15=
ENST00000256830.13:c.84_86delinsTGG	ENSP00000256830.8:p.Ser28=
ENST00000356462.10:c.84_86delinsTGG	ENSP00000348847.5:p.Ser28=
ENST00000357895.9:c.60_62delinsTGG	ENSP00000350569.4:p.Ser20=
ENST00000382850.8:c.84_86delinsTGG	ENSP00000372301.3:p.Ser28=
ENST00000400345.7:c.84_86delinsTGG	ENSP00000383199.2:p.Ser28=
ENST00000435432.6:c.-358_-356delinsTGG	ENSP00000393395.1:n.-358_-356delinsTGG
ENST00000456986.5:c.-280_-278delinsTGG	ENSP00000411947.1:n.-280_-278delinsTGG
ENST00000585363.5:n.121_123delinsTGG
ENST00000585594.5:n.204_206delinsTGG
ENST00000586263.5:c.60_62delinsTGG	ENSP00000468546.1:p.Ser20=
ENST00000587547.1:n.873_875delinsTGG
ENST00000588516.5:n.1184_1186delinsTGG
ENST00000589054.5:c.48+121115_48+121117delinsTGG	ENSP00000465669.1:n.48+121115_48+121117delinsTGG
ENST00000590694.5:n.127_129delinsTGG
ENST00000591579.5:n.128_130delinsTGG
ENST00000591989.5:n.132_134delinsTGG
ENST00000592846.5:c.-339_-337delinsTGG	ENSP00000466776.1:n.-339_-337delinsTGG
NM_001144964.1:c.-280_-278delinsTGG	NP_001138436.1:n.-280_-278delinsTGG
NM_001144965.1:c.-280_-278delinsTGG	NP_001138437.1:n.-280_-278delinsTGG
NM_001144967.2:c.84_86delinsTGG	NP_001138439.1:p.Ser28=
NM_001144968.1:c.60_62delinsTGG	NP_001138440.1:p.Ser20=
NM_001144969.1:c.60_62delinsTGG	NP_001138441.1:p.Ser20=
NM_001144971.1:c.-358_-356delinsTGG	NP_001138443.1:n.-358_-356delinsTGG
NM_001243960.1:c.84_86delinsTGG	NP_001230889.1:p.Ser28=
NM_015277.5:c.84_86delinsTGG	NP_056092.2:p.Ser28=
XM_006722426.2:c.84_86delinsTGG	XP_006722489.1:p.Ser28=
XM_006722428.2:c.84_86delinsTGG	XP_006722491.1:p.Ser28=
XM_011525887.1:c.60_62delinsTGG	XP_011524189.1:p.Ser20=
XM_006722426.4:c.84_86delinsTGG	XP_006722489.1:p.Ser28=
XM_006722428.4:c.84_86delinsTGG	XP_006722491.1:p.Ser28=
XM_011525887.3:c.60_62delinsTGG	XP_011524189.1:p.Ser20=
XM_017025678.2:c.84_86delinsTGG	XP_016881167.1:p.Ser28=
XM_024451129.1:c.-358_-356delinsTGG	XP_024306897.1:n.-358_-356delinsTGG
XM_024451131.1:c.-280_-278delinsTGG	XP_024306899.1:n.-280_-278delinsTGG
XM_024451134.1:c.-339_-337delinsTGG	XP_024306902.1:n.-339_-337delinsTGG
XM_024451135.1:c.-280_-278delinsTGG	XP_024306903.1:n.-280_-278delinsTGG
XM_024451136.1:c.-280_-278delinsTGG	XP_024306904.1:n.-280_-278delinsTGG
XM_024451137.1:c.-358_-356delinsTGG	XP_024306905.1:n.-358_-356delinsTGG
NM_001144967.3:c.84_86delinsTGG MANE Select	NP_001138439.1:p.Ser28=
NM_001144965.2:c.-280_-278delinsTGG	NP_001138437.1:n.-280_-278delinsTGG
NM_001144968.2:c.60_62delinsTGG	NP_001138440.1:p.Ser20=
NM_001144969.2:c.60_62delinsTGG	NP_001138441.1:p.Ser20=
NM_001144971.2:c.-358_-356delinsTGG	NP_001138443.1:n.-358_-356delinsTGG
NM_001243960.2:c.84_86delinsTGG	NP_001230889.1:p.Ser28=
NM_015277.6:c.84_86delinsTGG	NP_056092.2:p.Ser28=