LDH info

Canonical Allele Identifier: CA15159066
Gene: ZNF142 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10187066

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218650036A>G , CM000664.2:g.218650036A>G GRCh38
NC_000002.11:g.219514759A>G , CM000664.1:g.219514759A>G GRCh37
NC_000002.10:g.219223003A>G NCBI36
NG_033099.1:g.14505T>C

Transcript Alleles

HGVS Amino-acid change
NM_001105537.2:c.448+323T>C VV NP_001099007.1:p.=
NR_073599.1:n.1195+323T>C
NR_073600.1:n.1028+323T>C
XM_006712730.2:c.1048+323T>C XP_006712793.1:p.=
XM_011511784.1:c.1048+323T>C XP_011510086.1:p.=
XM_011511785.1:c.1048+323T>C XP_011510087.1:p.=
XM_011511786.1:c.1048+323T>C XP_011510088.1:p.=
XM_011511787.1:c.1048+323T>C XP_011510089.1:p.=
XM_011511788.1:c.1048+323T>C XP_011510090.1:p.=
XM_011511789.1:c.448+323T>C XP_011510091.1:p.=
NM_001366287.1:c.-42+323T>C VV NP_001353216.1:p.=
NM_001366288.1:c.-42+323T>C VV NP_001353217.1:p.=
NM_001366289.1:c.-42+323T>C VV NP_001353218.1:p.=
NM_001366290.1:c.1048+323T>C VV NP_001353219.1:p.=
NM_001366291.1:c.448+323T>C VV NP_001353220.1:p.=
XM_006712730.3:c.1048+323T>C XP_006712793.1:p.=
XM_011511784.2:c.1048+323T>C XP_011510086.1:p.=
XM_011511785.2:c.1048+323T>C XP_011510087.1:p.=
XM_011511786.2:c.1048+323T>C XP_011510088.1:p.=
XM_011511787.2:c.1048+323T>C XP_011510089.1:p.=
XM_011511788.2:c.1048+323T>C XP_011510090.1:p.=
XM_011511789.2:c.448+323T>C XP_011510091.1:p.=
NM_001105537.3:c.448+323T>C VV NP_001099007.1:p.=
NM_001105537.4:c.448+323T>C VV NP_001099007.1:p.=
NM_001366287.2:c.-42+323T>C VV NP_001353216.1:p.=
NM_001366288.2:c.-42+323T>C VV NP_001353217.1:p.=
NM_001366289.2:c.-42+323T>C VV NP_001353218.1:p.=
NM_001366290.3:c.1048+323T>C VV NP_001353219.1:p.=
NM_001366291.2:c.448+323T>C VV NP_001353220.1:p.=
ENST00000411696.6:c.448+323T>C ENSP00000398798.2:p.=
ENST00000433921.5:c.*273+323T>C ENSP00000405477.1:p.=
ENST00000449707.5:c.448+323T>C ENSP00000408643.1:p.=
ENST00000450765.5:c.*273+323T>C ENSP00000397456.1:p.=