Canonical Allele Identifier: CA400365840
Community Standard Title: NM_058216.3(RAD51C):c.1031A>G (p.Gln344Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734122A>G , CM000679.2:g.58734122A>G GRCh38
NC_000017.10:g.56811483A>G , CM000679.1:g.56811483A>G GRCh37
NC_000017.9:g.54166482A>G NCBI36
NG_023199.1:g.46521A>G , LRG_314:g.46521A>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1031A>G MANE Select NP_478123.1:p.Gln344Arg
ENST00000337432.9:c.1031A>G MANE Select ENSP00000336701.4:p.Gln344Arg
NM_058216.2:c.1031A>G NP_478123.1:p.Gln344Arg
NR_103872.1:n.935A>G
NR_103872.2:n.906A>G
ENST00000337432.8:c.1031A>G ENSP00000336701.4:p.Gln344Arg
ENST00000413590.5:c.672A>G
ENST00000461271.6:c.*1563A>G ENSP00000464056.2:n.*1563A>G
ENST00000461706.1:n.218A>G
ENST00000475762.5:c.*1667A>G ENSP00000432421.1:n.*1667A>G
ENST00000482007.5:c.*459A>G ENSP00000433332.1:n.*459A>G
ENST00000487525.5:c.*607A>G ENSP00000431637.1:n.*607A>G
ENST00000578151.1:n.244A>G
ENST00000581221.5:n.546A>G
ENST00000584804.1:c.265A>G ENSP00000463658.1:p.Arg89Gly
ENST00000697680.1:c.*1995A>G ENSP00000513392.1:n.*1995A>G
ENST00000697681.1:c.*2192A>G ENSP00000513393.1:n.*2192A>G
ENST00000697683.1:c.*1967A>G ENSP00000513395.1:n.*1967A>G
ENST00000697685.1:c.*1728A>G ENSP00000513396.1:n.*1728A>G
ENST00000697686.1:c.802A>G ENSP00000513397.1:p.Arg268Gly
ENST00000697689.1:c.*1445A>G ENSP00000513398.1:n.*1445A>G
ENST00000697690.1:c.909A>G ENSP00000513399.1:p.Ser303=
ENST00000697691.1:c.*1003A>G ENSP00000513400.1:n.*1003A>G
ENST00000697692.1:c.*1043A>G ENSP00000513401.1:n.*1043A>G
ENST00000697694.1:c.680A>G ENSP00000513402.1:p.Gln227Arg
ENST00000697695.1:n.1638A>G
XM_006722001.2:c.1034A>G XP_006722064.1:p.Gln345Arg
XM_006722001.4:c.1034A>G XP_006722064.1:p.Gln345Arg
XM_006722002.2:c.970A>G XP_006722065.1:p.Arg324Gly
XM_006722002.4:c.970A>G XP_006722065.1:p.Arg324Gly
XM_006722004.2:c.683A>G XP_006722067.1:p.Gln228Arg
XM_006722004.3:c.683A>G XP_006722067.1:p.Gln228Arg
XM_006722005.2:c.683A>G XP_006722068.1:p.Gln228Arg
XM_006722005.3:c.683A>G XP_006722068.1:p.Gln228Arg
XM_011525092.1:c.683A>G XP_011523394.1:p.Gln228Arg
XM_011525092.2:c.683A>G XP_011523394.1:p.Gln228Arg
XM_011525093.1:c.683A>G XP_011523395.1:p.Gln228Arg
XM_011525093.2:c.683A>G XP_011523395.1:p.Gln228Arg
XM_011525094.1:c.683A>G XP_011523396.1:p.Gln228Arg
XM_011525094.2:c.683A>G XP_011523396.1:p.Gln228Arg
XM_017024914.1:c.680A>G XP_016880403.1:p.Gln227Arg
XM_017024915.1:c.680A>G XP_016880404.1:p.Gln227Arg
XM_017024916.1:c.680A>G XP_016880405.1:p.Gln227Arg
XM_017024917.1:c.680A>G XP_016880406.1:p.Gln227Arg
XM_017024918.2:c.680A>G XP_016880407.1:p.Gln227Arg
XM_017024919.1:c.619A>G XP_016880408.1:p.Arg207Gly
XR_934513.1:n.1249A>G
XR_934513.3:n.1680A>G
XR_934514.1:n.1252A>G
XR_934514.3:n.1683A>G
XR_934886.1:n.149+3949T>C
XR_934886.2:n.149+3949T>C