LDH info

Canonical Allele Identifier: CA658683943
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 491545
ClinVar RCV Id: RCV000582521

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68738278T>C , CM000678.2:g.68738278T>C GRCh38
NC_000016.9:g.68772181T>C , CM000678.1:g.68772181T>C GRCh37
NC_000016.8:g.67329682T>C NCBI36
NG_008021.1:g.5987T>C , LRG_301:g.5987T>C

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.49-19T>C , LRG_301t1:c.49-19T>C NP_004351.1:p.=
NM_001317184.1:c.49-19T>C VV NP_001304113.1:p.=
NM_001317185.1:c.-1567-19T>C VV NP_001304114.1:p.=
NM_001317186.1:c.-1771-19T>C VV NP_001304115.1:p.=
NM_004360.4:c.49-19T>C VV NP_004351.1:p.=
NM_004360.5:c.49-19T>C VV MANE Preferred NP_004351.1:p.=
NM_001317184.2:c.49-19T>C VV NP_001304113.1:p.=
NM_001317185.2:c.-1567-19T>C VV NP_001304114.1:p.=
NM_001317186.2:c.-1771-19T>C VV NP_001304115.1:p.=
ENST00000261769.9:c.49-19T>C ENSP00000261769.4:p.=
ENST00000422392.6:c.49-19T>C ENSP00000414946.2:p.=
ENST00000566510.5:c.49-19T>C ENSP00000458139.1:p.=
ENST00000566612.5:c.49-19T>C ENSP00000454782.1:p.=
ENST00000611625.4:c.49-19T>C ENSP00000481063.1:p.=
ENST00000612417.4:c.49-19T>C ENSP00000478360.1:p.=
ENST00000621016.4:c.49-19T>C ENSP00000480664.1:p.=