LDH info

Canonical Allele Identifier: CA8975190
Gene: NEDD4L HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1008899

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58195615G>A , CM000680.2:g.58195615G>A GRCh38
NC_000018.9:g.55862847G>A , CM000680.1:g.55862847G>A GRCh37
NC_000018.8:g.54013845G>A NCBI36
NG_029954.1:g.156238G>A

Transcript Alleles

HGVS Amino-acid change
NM_001144964.1:c.-242+29754G>A VV NP_001138436.1:p.=
NM_001144965.1:c.-242+29754G>A VV NP_001138437.1:p.=
NM_001144967.2:c.122+29754G>A VV NP_001138439.1:p.=
NM_001144968.1:c.98+29754G>A VV NP_001138440.1:p.=
NM_001144969.1:c.98+29754G>A VV NP_001138441.1:p.=
NM_001144970.2:c.-360G>A VV NP_001138442.1:p.=
NM_001144971.1:c.-320+29754G>A VV NP_001138443.1:p.=
NM_001243960.1:c.122+29754G>A VV NP_001230889.1:p.=
NM_015277.5:c.122+29754G>A VV NP_056092.2:p.=
XM_006722426.2:c.122+29754G>A XP_006722489.1:p.=
XM_006722428.2:c.122+29754G>A XP_006722491.1:p.=
XM_006722430.2:c.-360G>A XP_006722493.1:p.=
XM_011525887.1:c.98+29754G>A XP_011524189.1:p.=
XR_935527.1:n.96C>T
XR_935528.1:n.96C>T
XR_935529.1:n.62C>T
XR_935530.1:n.82C>T
XM_006722426.4:c.122+29754G>A XP_006722489.1:p.=
XM_006722428.4:c.122+29754G>A XP_006722491.1:p.=
XM_006722430.4:c.-360G>A XP_006722493.1:p.=
XM_011525887.3:c.98+29754G>A XP_011524189.1:p.=
XM_017025678.2:c.122+29754G>A XP_016881167.1:p.=
XM_017025679.2:c.-360G>A XP_016881168.1:p.=
XM_017025680.2:c.-360G>A XP_016881169.1:p.=
XM_017025681.2:c.-360G>A XP_016881170.1:p.=
XM_024451129.1:c.-320+29754G>A XP_024306897.1:p.=
XM_024451131.1:c.-242+29754G>A XP_024306899.1:p.=
XM_024451134.1:c.-301+29754G>A XP_024306902.1:p.=
XM_024451135.1:c.-242+29754G>A XP_024306903.1:p.=
XM_024451136.1:c.-242+29754G>A XP_024306904.1:p.=
XM_024451137.1:c.-320+29754G>A XP_024306905.1:p.=
XR_935527.2:n.91C>T
XR_935528.2:n.91C>T
XR_935529.2:n.62C>T
NM_001144967.3:c.122+29754G>A VV MANE Preferred NP_001138439.1:p.=
ENST00000256830.13:n.122+29754G>A ENSP00000256830.8:p.=
ENST00000356462.10:c.122+29754G>A ENSP00000348847.5:p.=
ENST00000357895.9:c.98+29754G>A ENSP00000350569.4:p.=
ENST00000382850.8:c.122+29754G>A ENSP00000372301.3:p.=
ENST00000400345.7:c.122+29754G>A ENSP00000383199.2:p.=
ENST00000435432.6:c.-320+29754G>A ENSP00000393395.1:p.=
ENST00000456173.6:c.-360G>A ENSP00000405440.1:p.=
ENST00000456986.5:c.-242+29754G>A ENSP00000411947.1:p.=
ENST00000585363.5:n.159+29754G>A
ENST00000586263.5:c.98+29754G>A ENSP00000468546.1:p.=
ENST00000588516.5:n.1222+29754G>A
ENST00000589054.5:c.48+150907G>A ENSP00000465669.1:p.=
ENST00000591989.5:n.170+29754G>A
ENST00000592846.5:c.-301+29754G>A ENSP00000466776.1:p.=