LDH info

Canonical Allele Identifier: CA283320271
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13689

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68834619T>G , CM000678.2:g.68834619T>G GRCh38
NC_000016.9:g.68868522T>G , CM000678.1:g.68868522T>G GRCh37
NC_000016.8:g.67426023T>G NCBI36
NG_008021.1:g.102328T>G , LRG_301:g.102328T>G

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.*1120T>G , LRG_301t1:c.*1120T>G NP_004351.1:p.=
XM_011523488.1:c.*1120T>G XP_011521790.1:p.=
XM_011523489.1:c.*1120T>G XP_011521791.1:p.=
NM_001317184.1:c.*1120T>G VV NP_001304113.1:p.=
NM_001317185.1:c.*1120T>G VV NP_001304114.1:p.=
NM_001317186.1:c.*1120T>G VV NP_001304115.1:p.=
NM_004360.4:c.*1120T>G VV NP_004351.1:p.=
NM_004360.5:c.*1120T>G VV MANE Preferred NP_004351.1:p.=
NM_001317184.2:c.*1120T>G VV NP_001304113.1:p.=
NM_001317185.2:c.*1120T>G VV NP_001304114.1:p.=
NM_001317186.2:c.*1120T>G VV NP_001304115.1:p.=
ENST00000261769.9:c.*1120T>G ENSP00000261769.4:p.=
ENST00000566612.5:c.*2009T>G ENSP00000454782.1:p.=
ENST00000611625.4:c.*1120T>G ENSP00000481063.1:p.=
ENST00000621016.4:c.*338T>G ENSP00000480664.1:p.=