LDH info

Canonical Allele Identifier: CA164689486
Gene: COG5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3815148

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107297975A>C , CM000669.2:g.107297975A>C GRCh38
NC_000007.13:g.106938420A>C , CM000669.1:g.106938420A>C GRCh37
NC_000007.12:g.106725656A>C NCBI36
NG_028095.1:g.271540T>G
NG_028095.2:g.271540T>G

Transcript Alleles

HGVS Amino-acid change
NM_001161520.1:c.1406+167T>G VV NP_001154992.1:p.=
NM_006348.3:c.1406+167T>G VV NP_006339.3:p.=
NM_181733.2:c.1406+167T>G VV NP_859422.2:p.=
XM_011515738.1:c.1406+167T>G XP_011514040.1:p.=
XM_024446634.1:c.1406+167T>G XP_024302402.1:p.=
NM_001161520.2:c.1313+167T>G VV NP_001154992.2:p.=
NM_006348.4:c.1313+167T>G VV NP_006339.4:p.=
NM_181733.3:c.1313+167T>G VV NP_859422.3:p.=
NM_001379511.1:c.1313+167T>G VV NP_001366440.1:p.=
NM_001379512.1:c.1313+167T>G VV NP_001366441.1:p.=
NM_001379513.1:c.1313+167T>G VV NP_001366442.1:p.=
NM_001379514.1:c.1313+167T>G VV NP_001366443.1:p.=
NM_001379515.1:c.743+167T>G VV NP_001366444.1:p.=
NM_001379516.1:c.599+167T>G VV NP_001366445.1:p.=
NM_006348.5:c.1313+167T>G VV NP_006339.4:p.=
NM_181733.4:c.1313+167T>G VV NP_859422.3:p.=
ENST00000297135.7:c.1406+167T>G ENSP00000297135.3:p.=
ENST00000347053.7:c.1406+167T>G ENSP00000334703.2:p.=
ENST00000393603.6:c.1406+167T>G ENSP00000377228.2:p.=