Canonical Allele Identifier: CA2306321798

Gene: NEDD4L

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58149568_58149569delinsCG , CM000680.2:g.58149568_58149569delinsCG	GRCh38
NC_000018.9:g.55816800_55816801delinsCG , CM000680.1:g.55816800_55816801delinsCG	GRCh37
NC_000018.8:g.53967798_53967799delinsCG	NCBI36
NG_029954.1:g.110191_110192delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400345.8:c.49-16220_49-16219delinsCG MANE Select	ENSP00000383199.2:n.49-16220_49-16219delinsCG
ENST00000585594.6:n.26-16220_26-16219delinsCG
ENST00000674613.1:n.98-95859_98-95858delinsCG
ENST00000674845.1:c.*555-16220_*555-16219delinsCG	ENSP00000502309.1:n.*555-16220_*555-16219delinsCG
ENST00000675137.1:n.171-16220_171-16219delinsCG
ENST00000675147.1:c.28-16220_28-16219delinsCG	ENSP00000501840.1:n.28-16220_28-16219delinsCG
ENST00000675227.1:c.95-16220_95-16219delinsCG	ENSP00000502649.1:n.95-16220_95-16219delinsCG
ENST00000675502.1:c.-315-16220_-315-16219delinsCG	ENSP00000502428.1:n.-315-16220_-315-16219delinsCG
ENST00000675554.1:n.165-16220_165-16219delinsCG
ENST00000675801.1:c.-315-16220_-315-16219delinsCG	ENSP00000502688.1:n.-315-16220_-315-16219delinsCG
ENST00000676024.1:c.49-16220_49-16219delinsCG	ENSP00000502105.1:n.49-16220_49-16219delinsCG
ENST00000676223.1:c.10-16220_10-16219delinsCG	ENSP00000502361.1:n.10-16220_10-16219delinsCG
ENST00000256830.13:c.49-16220_49-16219delinsCG	ENSP00000256830.8:n.49-16220_49-16219delinsCG
ENST00000356462.10:c.49-16220_49-16219delinsCG	ENSP00000348847.5:n.49-16220_49-16219delinsCG
ENST00000357895.9:c.24+9_24+10delinsCG	ENSP00000350569.4:n.24+9_24+10delinsCG
ENST00000382850.8:c.49-16220_49-16219delinsCG	ENSP00000372301.3:n.49-16220_49-16219delinsCG
ENST00000400345.7:c.49-16220_49-16219delinsCG	ENSP00000383199.2:n.49-16220_49-16219delinsCG
ENST00000435432.6:c.-395_-394delinsCG	ENSP00000393395.1:n.-395_-394delinsCG
ENST00000456986.5:c.-315-16220_-315-16219delinsCG	ENSP00000411947.1:n.-315-16220_-315-16219delinsCG
ENST00000585363.5:n.86-16220_86-16219delinsCG
ENST00000585594.5:n.169-16220_169-16219delinsCG
ENST00000586263.5:c.24+9_24+10delinsCG	ENSP00000468546.1:n.24+9_24+10delinsCG
ENST00000587547.1:n.838-16220_838-16219delinsCG
ENST00000588516.5:n.1149-16220_1149-16219delinsCG
ENST00000589054.5:c.48+104860_48+104861delinsCG	ENSP00000465669.1:n.48+104860_48+104861delinsCG
ENST00000590694.5:n.92-16220_92-16219delinsCG
ENST00000591579.5:n.93-16220_93-16219delinsCG
ENST00000591989.5:n.101-16224_101-16223delinsCG
ENST00000592846.5:c.-370-16224_-370-16223delinsCG	ENSP00000466776.1:n.-370-16224_-370-16223delinsCG
NM_001144964.1:c.-315-16220_-315-16219delinsCG	NP_001138436.1:n.-315-16220_-315-16219delinsCG
NM_001144965.1:c.-317_-316delinsCG	NP_001138437.1:n.-317_-316delinsCG
NM_001144967.2:c.49-16220_49-16219delinsCG	NP_001138439.1:n.49-16220_49-16219delinsCG
NM_001144968.1:c.24+9_24+10delinsCG	NP_001138440.1:n.24+9_24+10delinsCG
NM_001144969.1:c.24+9_24+10delinsCG	NP_001138441.1:n.24+9_24+10delinsCG
NM_001144971.1:c.-395_-394delinsCG	NP_001138443.1:n.-395_-394delinsCG
NM_001243960.1:c.49-16220_49-16219delinsCG	NP_001230889.1:n.49-16220_49-16219delinsCG
NM_015277.5:c.49-16220_49-16219delinsCG	NP_056092.2:n.49-16220_49-16219delinsCG
XM_006722426.2:c.49-16220_49-16219delinsCG	XP_006722489.1:n.49-16220_49-16219delinsCG
XM_006722428.2:c.49-16220_49-16219delinsCG	XP_006722491.1:n.49-16220_49-16219delinsCG
XM_011525887.1:c.24+9_24+10delinsCG	XP_011524189.1:n.24+9_24+10delinsCG
XM_006722426.4:c.49-16220_49-16219delinsCG	XP_006722489.1:n.49-16220_49-16219delinsCG
XM_006722428.4:c.49-16220_49-16219delinsCG	XP_006722491.1:n.49-16220_49-16219delinsCG
XM_011525887.3:c.24+9_24+10delinsCG	XP_011524189.1:n.24+9_24+10delinsCG
XM_017025678.2:c.49-16220_49-16219delinsCG	XP_016881167.1:n.49-16220_49-16219delinsCG
XM_024451129.1:c.-393-16220_-393-16219delinsCG	XP_024306897.1:n.-393-16220_-393-16219delinsCG
XM_024451131.1:c.-315-16220_-315-16219delinsCG	XP_024306899.1:n.-315-16220_-315-16219delinsCG
XM_024451134.1:c.-376_-375delinsCG	XP_024306902.1:n.-376_-375delinsCG
XM_024451135.1:c.-315-16220_-315-16219delinsCG	XP_024306903.1:n.-315-16220_-315-16219delinsCG
XM_024451136.1:c.-315-16220_-315-16219delinsCG	XP_024306904.1:n.-315-16220_-315-16219delinsCG
XM_024451137.1:c.-393-16220_-393-16219delinsCG	XP_024306905.1:n.-393-16220_-393-16219delinsCG
NM_001144967.3:c.49-16220_49-16219delinsCG MANE Select	NP_001138439.1:n.49-16220_49-16219delinsCG
NM_001144965.2:c.-317_-316delinsCG	NP_001138437.1:n.-317_-316delinsCG
NM_001144968.2:c.24+9_24+10delinsCG	NP_001138440.1:n.24+9_24+10delinsCG
NM_001144969.2:c.24+9_24+10delinsCG	NP_001138441.1:n.24+9_24+10delinsCG
NM_001144971.2:c.-395_-394delinsCG	NP_001138443.1:n.-395_-394delinsCG
NM_001243960.2:c.49-16220_49-16219delinsCG	NP_001230889.1:n.49-16220_49-16219delinsCG
NM_015277.6:c.49-16220_49-16219delinsCG	NP_056092.2:n.49-16220_49-16219delinsCG