Canonical Allele Identifier: CA400366005
Community Standard Title: NM_058216.3(RAD51C):c.1047T>G (p.Thr349=)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734138T>G , CM000679.2:g.58734138T>G GRCh38
NC_000017.10:g.56811499T>G , CM000679.1:g.56811499T>G GRCh37
NC_000017.9:g.54166498T>G NCBI36
NG_023199.1:g.46537T>G , LRG_314:g.46537T>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1047T>G MANE Select NP_478123.1:p.Thr349=
ENST00000337432.9:c.1047T>G MANE Select ENSP00000336701.4:p.Thr349=
NM_058216.2:c.1047T>G NP_478123.1:p.Thr349=
NR_103872.1:n.951T>G
NR_103872.2:n.922T>G
ENST00000337432.8:c.1047T>G ENSP00000336701.4:p.Thr349=
ENST00000413590.5:c.688T>G
ENST00000461271.6:c.*1579T>G ENSP00000464056.2:n.*1579T>G
ENST00000461706.1:n.234T>G
ENST00000475762.5:c.*1683T>G ENSP00000432421.1:n.*1683T>G
ENST00000482007.5:c.*475T>G ENSP00000433332.1:n.*475T>G
ENST00000487525.5:c.*623T>G ENSP00000431637.1:n.*623T>G
ENST00000578151.1:n.260T>G
ENST00000581221.5:n.562T>G
ENST00000584804.1:c.281T>G ENSP00000463658.1:p.Leu94Arg
ENST00000697680.1:c.*2011T>G ENSP00000513392.1:n.*2011T>G
ENST00000697681.1:c.*2208T>G ENSP00000513393.1:n.*2208T>G
ENST00000697683.1:c.*1983T>G ENSP00000513395.1:n.*1983T>G
ENST00000697685.1:c.*1744T>G ENSP00000513396.1:n.*1744T>G
ENST00000697686.1:c.818T>G ENSP00000513397.1:p.Leu273Arg
ENST00000697689.1:c.*1461T>G ENSP00000513398.1:n.*1461T>G
ENST00000697690.1:c.*7T>G ENSP00000513399.1:n.*7T>G
ENST00000697691.1:c.*1019T>G ENSP00000513400.1:n.*1019T>G
ENST00000697692.1:c.*1059T>G ENSP00000513401.1:n.*1059T>G
ENST00000697694.1:c.696T>G ENSP00000513402.1:p.Thr232=
ENST00000697695.1:n.1654T>G
XM_006722001.2:c.1050T>G XP_006722064.1:p.Thr350=
XM_006722001.4:c.1050T>G XP_006722064.1:p.Thr350=
XM_006722002.2:c.986T>G XP_006722065.1:p.Leu329Arg
XM_006722002.4:c.986T>G XP_006722065.1:p.Leu329Arg
XM_006722004.2:c.699T>G XP_006722067.1:p.Thr233=
XM_006722004.3:c.699T>G XP_006722067.1:p.Thr233=
XM_006722005.2:c.699T>G XP_006722068.1:p.Thr233=
XM_006722005.3:c.699T>G XP_006722068.1:p.Thr233=
XM_011525092.1:c.699T>G XP_011523394.1:p.Thr233=
XM_011525092.2:c.699T>G XP_011523394.1:p.Thr233=
XM_011525093.1:c.699T>G XP_011523395.1:p.Thr233=
XM_011525093.2:c.699T>G XP_011523395.1:p.Thr233=
XM_011525094.1:c.699T>G XP_011523396.1:p.Thr233=
XM_011525094.2:c.699T>G XP_011523396.1:p.Thr233=
XM_017024914.1:c.696T>G XP_016880403.1:p.Thr232=
XM_017024915.1:c.696T>G XP_016880404.1:p.Thr232=
XM_017024916.1:c.696T>G XP_016880405.1:p.Thr232=
XM_017024917.1:c.696T>G XP_016880406.1:p.Thr232=
XM_017024918.2:c.696T>G XP_016880407.1:p.Thr232=
XM_017024919.1:c.635T>G XP_016880408.1:p.Leu212Arg
XR_934513.1:n.1265T>G
XR_934513.3:n.1696T>G
XR_934514.1:n.1268T>G
XR_934514.3:n.1699T>G
XR_934886.1:n.149+3933A>C
XR_934886.2:n.149+3933A>C