LDH info

Canonical Allele Identifier: CA332999
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 136155
dbSNP Id: rs587780835

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734116A>G , CM000679.2:g.58734116A>G GRCh38
NC_000017.10:g.56811477A>G , CM000679.1:g.56811477A>G GRCh37
NC_000017.9:g.54166476A>G NCBI36
NG_023199.1:g.46515A>G , LRG_314:g.46515A>G

Transcript Alleles

HGVS Amino-acid change
NM_058216.2:c.1027-2A>G VV NP_478123.1:p.=
NR_103872.1:n.931-2A>G
XM_006722001.2:c.1030-2A>G XP_006722064.1:p.=
XM_006722002.2:c.966-2A>G XP_006722065.1:p.=
XM_006722004.2:c.679-2A>G XP_006722067.1:p.=
XM_006722005.2:c.679-2A>G XP_006722068.1:p.=
XM_011525092.1:c.679-2A>G XP_011523394.1:p.=
XM_011525093.1:c.679-2A>G XP_011523395.1:p.=
XM_011525094.1:c.679-2A>G XP_011523396.1:p.=
XR_934513.1:n.1245-2A>G
XR_934514.1:n.1248-2A>G
XR_934886.1:n.149+3955T>C
XM_006722001.4:c.1030-2A>G XP_006722064.1:p.=
XM_006722002.4:c.966-2A>G XP_006722065.1:p.=
XM_006722004.3:c.679-2A>G XP_006722067.1:p.=
XM_006722005.3:c.679-2A>G XP_006722068.1:p.=
XM_011525092.2:c.679-2A>G XP_011523394.1:p.=
XM_011525093.2:c.679-2A>G XP_011523395.1:p.=
XM_011525094.2:c.679-2A>G XP_011523396.1:p.=
XM_017024914.1:c.676-2A>G XP_016880403.1:p.=
XM_017024915.1:c.676-2A>G XP_016880404.1:p.=
XM_017024916.1:c.676-2A>G XP_016880405.1:p.=
XM_017024917.1:c.676-2A>G XP_016880406.1:p.=
XM_017024918.2:c.676-2A>G XP_016880407.1:p.=
XM_017024919.1:c.615-2A>G XP_016880408.1:p.=
XR_934513.3:n.1676-2A>G
XR_934514.3:n.1679-2A>G
XR_934886.2:n.149+3955T>C
NM_058216.3:c.1027-2A>G VV MANE Preferred NP_478123.1:p.=
NR_103872.2:n.902-2A>G
ENST00000337432.8:c.1027-2A>G ENSP00000336701.4:p.=
ENST00000413590.5:n.668-2A>G
ENST00000461706.1:n.214-2A>G
ENST00000475762.5:c.*1663-2A>G ENSP00000432421.1:p.=
ENST00000482007.5:c.*455-2A>G ENSP00000433332.1:p.=
ENST00000487525.5:c.*603-2A>G ENSP00000431637.1:p.=
ENST00000578151.1:n.240-2A>G
ENST00000581221.5:n.542-2A>G
ENST00000584804.1:n.261-2A>G ENSP00000463658.1:p.=