LDH info

Canonical Allele Identifier: CA8677103
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 324173
dbSNP Id: rs12946397

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692618C>T , CM000679.2:g.58692618C>T GRCh38
NC_000017.10:g.56769979C>T , CM000679.1:g.56769979C>T GRCh37
NC_000017.9:g.54124978C>T NCBI36
NG_023199.1:g.5017C>T , LRG_314:g.5017C>T
NG_047169.1:g.4462G>A

Transcript Alleles

HGVS Amino-acid change
NM_002876.3:c.-26C>T VV NP_002867.1:p.=
NM_058216.2:c.-26C>T VV NP_478123.1:p.=
NR_103872.1:n.46C>T
NR_103873.1:n.46C>T
XM_006722001.2:c.-26C>T XP_006722064.1:p.=
XM_006722002.2:c.-26C>T XP_006722065.1:p.=
XM_006722004.2:c.-274C>T XP_006722067.1:p.=
XM_006722005.2:c.-221C>T XP_006722068.1:p.=
XM_011525092.1:c.-574C>T XP_011523394.1:p.=
XM_011525093.1:c.-735C>T XP_011523395.1:p.=
XR_934513.1:n.48C>T
XR_934514.1:n.48C>T
XM_006722001.4:c.-26C>T XP_006722064.1:p.=
XM_006722002.4:c.-26C>T XP_006722065.1:p.=
XM_006722004.3:c.-274C>T XP_006722067.1:p.=
XM_006722005.3:c.-221C>T XP_006722068.1:p.=
XM_017024914.1:c.-274C>T XP_016880403.1:p.=
XM_017024916.1:c.-574C>T XP_016880405.1:p.=
XM_017024917.1:c.-221C>T XP_016880406.1:p.=
XR_934513.3:n.479C>T
XR_934514.3:n.479C>T
NM_058216.3:c.-26C>T VV MANE Preferred NP_478123.1:p.=
NR_103872.2:n.17C>T
ENST00000337432.8:c.-26C>T ENSP00000336701.4:p.=
ENST00000461271.5:c.-274C>T ENSP00000464056.1:p.=
ENST00000475762.5:c.-26C>T ENSP00000432421.1:p.=
ENST00000476741.2:n.17C>T
ENST00000482007.5:c.-26C>T ENSP00000433332.1:p.=
ENST00000486827.1:c.-26C>T ENSP00000436761.1:p.=
ENST00000487525.5:c.-26C>T ENSP00000431637.1:p.=
ENST00000487921.5:n.43C>T
ENST00000583539.5:c.-26C>T ENSP00000463121.1:p.=