LDH info

Canonical Allele Identifier: CA283318253
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs754162869

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829668C>G , CM000678.2:g.68829668C>G GRCh38
NC_000016.9:g.68863571C>G , CM000678.1:g.68863571C>G GRCh37
NC_000016.8:g.67421072C>G NCBI36
NG_008021.1:g.97377C>G , LRG_301:g.97377C>G

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.2310C>G , LRG_301t1:c.2310C>G NP_004351.1:p.Ser770Arg
XM_011523488.1:c.1575C>G XP_011521790.1:p.Ser525Arg
XM_011523489.1:c.1575C>G XP_011521791.1:p.Ser525Arg
NM_001317184.1:c.2127C>G VV NP_001304113.1:p.Ser709Arg
NM_001317185.1:c.762C>G VV NP_001304114.1:p.Ser254Arg
NM_001317186.1:c.345C>G VV NP_001304115.1:p.Ser115Arg
NM_004360.4:c.2310C>G VV NP_004351.1:p.Ser770Arg
NM_004360.5:c.2310C>G VV MANE Preferred NP_004351.1:p.Ser770Arg
ENST00000261769.9:c.2310C>G ENSP00000261769.4:p.Ser770Arg
ENST00000422392.6:c.2127C>G ENSP00000414946.2:p.Ser709Arg
ENST00000562118.1:n.528C>G
ENST00000562836.5:n.2381C>G
ENST00000566510.5:c.*976C>G ENSP00000458139.1:p.=
ENST00000566612.5:c.*550C>G ENSP00000454782.1:p.=
ENST00000611625.4:c.2373C>G ENSP00000481063.1:p.Ser791Arg
ENST00000612417.4:c.1853+3114C>G ENSP00000478360.1:p.=
ENST00000621016.4:c.1866-4535C>G ENSP00000480664.1:p.=