Canonical Allele Identifier: CA402715263

Gene: NEDD4L

Linked Data

• MyVariant Identifiers: chr18:g.55833051T>G (hg19) ; chr18:g.58165819T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58165819T>G , CM000680.2:g.58165819T>G	GRCh38
NC_000018.9:g.55833051T>G , CM000680.1:g.55833051T>G	GRCh37
NC_000018.8:g.53984049T>G	NCBI36
NG_029954.1:g.126442T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400345.8:c.80T>G MANE Select	ENSP00000383199.2:p.Val27Gly
ENST00000585594.6:n.57T>G
ENST00000674613.1:n.98-79608T>G
ENST00000674845.1:c.*586T>G	ENSP00000502309.1:n.*586T>G
ENST00000675137.1:n.202T>G
ENST00000675147.1:c.59T>G	ENSP00000501840.1:p.Val20Gly
ENST00000675502.1:c.-284T>G	ENSP00000502428.1:n.-284T>G
ENST00000675801.1:c.-284T>G	ENSP00000502688.1:n.-284T>G
ENST00000676024.1:c.80T>G	ENSP00000502105.1:p.Val27Gly
ENST00000676223.1:c.41T>G	ENSP00000502361.1:p.Val14Gly
ENST00000256830.13:c.80T>G	ENSP00000256830.8:p.Val27Gly
ENST00000356462.10:c.80T>G	ENSP00000348847.5:p.Val27Gly
ENST00000357895.9:c.56T>G	ENSP00000350569.4:p.Val19Gly
ENST00000382850.8:c.80T>G	ENSP00000372301.3:p.Val27Gly
ENST00000400345.7:c.80T>G	ENSP00000383199.2:p.Val27Gly
ENST00000435432.6:c.-362T>G	ENSP00000393395.1:n.-362T>G
ENST00000456986.5:c.-284T>G	ENSP00000411947.1:n.-284T>G
ENST00000585363.5:n.117T>G
ENST00000585594.5:n.200T>G
ENST00000586263.5:c.56T>G	ENSP00000468546.1:p.Val19Gly
ENST00000587547.1:n.869T>G
ENST00000588516.5:n.1180T>G
ENST00000589054.5:c.48+121111T>G	ENSP00000465669.1:n.48+121111T>G
ENST00000590694.5:n.123T>G
ENST00000591579.5:n.124T>G
ENST00000591989.5:n.128T>G
ENST00000592846.5:c.-343T>G	ENSP00000466776.1:n.-343T>G
NM_001144964.1:c.-284T>G	NP_001138436.1:n.-284T>G
NM_001144965.1:c.-284T>G	NP_001138437.1:n.-284T>G
NM_001144967.2:c.80T>G	NP_001138439.1:p.Val27Gly
NM_001144968.1:c.56T>G	NP_001138440.1:p.Val19Gly
NM_001144969.1:c.56T>G	NP_001138441.1:p.Val19Gly
NM_001144971.1:c.-362T>G	NP_001138443.1:n.-362T>G
NM_001243960.1:c.80T>G	NP_001230889.1:p.Val27Gly
NM_015277.5:c.80T>G	NP_056092.2:p.Val27Gly
XM_006722426.2:c.80T>G	XP_006722489.1:p.Val27Gly
XM_006722428.2:c.80T>G	XP_006722491.1:p.Val27Gly
XM_011525887.1:c.56T>G	XP_011524189.1:p.Val19Gly
XM_006722426.4:c.80T>G	XP_006722489.1:p.Val27Gly
XM_006722428.4:c.80T>G	XP_006722491.1:p.Val27Gly
XM_011525887.3:c.56T>G	XP_011524189.1:p.Val19Gly
XM_017025678.2:c.80T>G	XP_016881167.1:p.Val27Gly
XM_024451129.1:c.-362T>G	XP_024306897.1:n.-362T>G
XM_024451131.1:c.-284T>G	XP_024306899.1:n.-284T>G
XM_024451134.1:c.-343T>G	XP_024306902.1:n.-343T>G
XM_024451135.1:c.-284T>G	XP_024306903.1:n.-284T>G
XM_024451136.1:c.-284T>G	XP_024306904.1:n.-284T>G
XM_024451137.1:c.-362T>G	XP_024306905.1:n.-362T>G
NM_001144967.3:c.80T>G MANE Select	NP_001138439.1:p.Val27Gly
NM_001144965.2:c.-284T>G	NP_001138437.1:n.-284T>G
NM_001144968.2:c.56T>G	NP_001138440.1:p.Val19Gly
NM_001144969.2:c.56T>G	NP_001138441.1:p.Val19Gly
NM_001144971.2:c.-362T>G	NP_001138443.1:n.-362T>G
NM_001243960.2:c.80T>G	NP_001230889.1:p.Val27Gly
NM_015277.6:c.80T>G	NP_056092.2:p.Val27Gly