LDH info

Canonical Allele Identifier: CA299893
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 182838
dbSNP Id: rs730881933

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724101G>A , CM000679.2:g.58724101G>A GRCh38
NC_000017.10:g.56801462G>A , CM000679.1:g.56801462G>A GRCh37
NC_000017.9:g.54156461G>A NCBI36
NG_023199.1:g.36500G>A , LRG_314:g.36500G>A

Transcript Alleles

HGVS Amino-acid change
NM_058216.2:c.965+1G>A VV NP_478123.1:p.=
NR_103872.1:n.869+1G>A
XM_006722001.2:c.965+1G>A XP_006722064.1:p.=
XM_006722002.2:c.904+3289G>A XP_006722065.1:p.=
XM_006722004.2:c.614+1G>A XP_006722067.1:p.=
XM_006722005.2:c.614+1G>A XP_006722068.1:p.=
XM_011525092.1:c.614+1G>A XP_011523394.1:p.=
XM_011525093.1:c.614+1G>A XP_011523395.1:p.=
XM_011525094.1:c.614+1G>A XP_011523396.1:p.=
XR_934513.1:n.1183+1G>A
XR_934514.1:n.1183+1G>A
XM_006722001.4:c.965+1G>A XP_006722064.1:p.=
XM_006722002.4:c.904+3289G>A XP_006722065.1:p.=
XM_006722004.3:c.614+1G>A XP_006722067.1:p.=
XM_006722005.3:c.614+1G>A XP_006722068.1:p.=
XM_011525092.2:c.614+1G>A XP_011523394.1:p.=
XM_011525093.2:c.614+1G>A XP_011523395.1:p.=
XM_011525094.2:c.614+1G>A XP_011523396.1:p.=
XM_017024914.1:c.614+1G>A XP_016880403.1:p.=
XM_017024915.1:c.614+1G>A XP_016880404.1:p.=
XM_017024916.1:c.614+1G>A XP_016880405.1:p.=
XM_017024917.1:c.614+1G>A XP_016880406.1:p.=
XM_017024918.2:c.614+1G>A XP_016880407.1:p.=
XM_017024919.1:c.553+3289G>A XP_016880408.1:p.=
XR_934513.3:n.1614+1G>A
XR_934514.3:n.1614+1G>A
NM_058216.3:c.965+1G>A VV MANE Preferred NP_478123.1:p.=
NR_103872.2:n.840+1G>A
ENST00000337432.8:c.965+1G>A ENSP00000336701.4:p.=
ENST00000413590.5:n.603+1G>A
ENST00000475762.5:c.*1601+1G>A ENSP00000432421.1:p.=
ENST00000482007.5:c.*393+1G>A ENSP00000433332.1:p.=
ENST00000487525.5:c.*538+1G>A ENSP00000431637.1:p.=
ENST00000578151.1:n.239+3289G>A
ENST00000581221.5:n.480+1G>A
ENST00000583539.5:c.965+1G>A ENSP00000463121.1:p.=
ENST00000584617.5:n.687+1G>A
ENST00000584804.1:n.199+3289G>A ENSP00000463658.1:p.=