LDH info

Canonical Allele Identifier: CA501074380
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr17:g.56770109T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692748T>G , CM000679.2:g.58692748T>G GRCh38
NC_000017.10:g.56770109T>G , CM000679.1:g.56770109T>G GRCh37
NC_000017.9:g.54125108T>G NCBI36
NG_023199.1:g.5147T>G , LRG_314:g.5147T>G
NG_047169.1:g.4332A>C

Transcript Alleles

HGVS Amino-acid change
NM_002876.3:c.105T>G VV NP_002867.1:p.Ala35=
NM_058216.2:c.105T>G VV NP_478123.1:p.Ala35=
NR_103872.1:n.176T>G
NR_103873.1:n.113+63T>G
XM_006722001.2:c.105T>G XP_006722064.1:p.Ala35=
XM_006722002.2:c.105T>G XP_006722065.1:p.Ala35=
XM_006722004.2:c.-207+63T>G XP_006722067.1:p.=
XM_006722005.2:c.-207+116T>G XP_006722068.1:p.=
XM_011525092.1:c.-507+63T>G XP_011523394.1:p.=
XM_011525093.1:c.-668+63T>G XP_011523395.1:p.=
XR_934513.1:n.178T>G
XR_934514.1:n.178T>G
XM_006722001.4:c.105T>G XP_006722064.1:p.Ala35=
XM_006722002.4:c.105T>G XP_006722065.1:p.Ala35=
XM_006722004.3:c.-207+63T>G XP_006722067.1:p.=
XM_006722005.3:c.-207+116T>G XP_006722068.1:p.=
XM_011525092.2:c.-507+63T>G XP_011523394.1:p.=
XM_011525093.2:c.-668+63T>G XP_011523395.1:p.=
XM_017024914.1:c.-207+63T>G XP_016880403.1:p.=
XM_017024916.1:c.-507+63T>G XP_016880405.1:p.=
XM_017024917.1:c.-207+116T>G XP_016880406.1:p.=
XM_017024918.2:c.-418T>G XP_016880407.1:p.=
XM_017024919.1:c.-668+63T>G XP_016880408.1:p.=
XR_934513.3:n.609T>G
XR_934514.3:n.609T>G
NM_058216.3:c.105T>G VV MANE Preferred NP_478123.1:p.Ala35=
ENST00000337432.8:c.105T>G ENSP00000336701.4:p.Ala35=
ENST00000421782.3:c.105T>G ENSP00000391450.2:p.Ala35=
ENST00000461271.5:c.-207+63T>G ENSP00000464056.1:p.=
ENST00000475762.5:c.105T>G ENSP00000432421.1:p.Ala35=
ENST00000476741.2:n.147T>G
ENST00000482007.5:c.105T>G ENSP00000433332.1:p.Ala35=
ENST00000486827.1:c.105T>G ENSP00000436761.1:p.Ala35=
ENST00000487525.5:c.105T>G ENSP00000431637.1:p.Ala35=
ENST00000487921.5:n.57+116T>G
ENST00000583539.5:c.105T>G ENSP00000463121.1:p.Ala35=
ENST00000584617.5:n.86T>G