LDH info

Canonical Allele Identifier: CA16608220
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 384788
ClinVar RCV Id: RCV000432573

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738282T>A , CM000678.2:g.68738282T>A GRCh38
NC_000016.9:g.68772185T>A , CM000678.1:g.68772185T>A GRCh37
NC_000016.8:g.67329686T>A NCBI36
NG_008021.1:g.5991T>A , LRG_301:g.5991T>A

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.49-15T>A , LRG_301t1:c.49-15T>A NP_004351.1:p.=
NM_001317184.1:c.49-15T>A VV NP_001304113.1:p.=
NM_001317185.1:c.-1567-15T>A VV NP_001304114.1:p.=
NM_001317186.1:c.-1771-15T>A VV NP_001304115.1:p.=
NM_004360.4:c.49-15T>A VV NP_004351.1:p.=
NM_004360.5:c.49-15T>A VV MANE Preferred NP_004351.1:p.=
NM_001317184.2:c.49-15T>A VV NP_001304113.1:p.=
NM_001317185.2:c.-1567-15T>A VV NP_001304114.1:p.=
NM_001317186.2:c.-1771-15T>A VV NP_001304115.1:p.=
ENST00000261769.9:c.49-15T>A ENSP00000261769.4:p.=
ENST00000422392.6:c.49-15T>A ENSP00000414946.2:p.=
ENST00000566510.5:c.49-15T>A ENSP00000458139.1:p.=
ENST00000566612.5:c.49-15T>A ENSP00000454782.1:p.=
ENST00000611625.4:c.49-15T>A ENSP00000481063.1:p.=
ENST00000612417.4:c.49-15T>A ENSP00000478360.1:p.=
ENST00000621016.4:c.49-15T>A ENSP00000480664.1:p.=