Canonical Allele Identifier: CA400365994
Community Standard Title: NM_058216.3(RAD51C):c.1045A>G (p.Thr349Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734136A>G , CM000679.2:g.58734136A>G GRCh38
NC_000017.10:g.56811497A>G , CM000679.1:g.56811497A>G GRCh37
NC_000017.9:g.54166496A>G NCBI36
NG_023199.1:g.46535A>G , LRG_314:g.46535A>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1045A>G MANE Select NP_478123.1:p.Thr349Ala
ENST00000337432.9:c.1045A>G MANE Select ENSP00000336701.4:p.Thr349Ala
NM_058216.2:c.1045A>G NP_478123.1:p.Thr349Ala
NR_103872.1:n.949A>G
NR_103872.2:n.920A>G
ENST00000337432.8:c.1045A>G ENSP00000336701.4:p.Thr349Ala
ENST00000413590.5:c.686A>G
ENST00000461271.6:c.*1577A>G ENSP00000464056.2:n.*1577A>G
ENST00000461706.1:n.232A>G
ENST00000475762.5:c.*1681A>G ENSP00000432421.1:n.*1681A>G
ENST00000482007.5:c.*473A>G ENSP00000433332.1:n.*473A>G
ENST00000487525.5:c.*621A>G ENSP00000431637.1:n.*621A>G
ENST00000578151.1:n.258A>G
ENST00000581221.5:n.560A>G
ENST00000584804.1:c.279A>G ENSP00000463658.1:p.Ile93Met
ENST00000697680.1:c.*2009A>G ENSP00000513392.1:n.*2009A>G
ENST00000697681.1:c.*2206A>G ENSP00000513393.1:n.*2206A>G
ENST00000697683.1:c.*1981A>G ENSP00000513395.1:n.*1981A>G
ENST00000697685.1:c.*1742A>G ENSP00000513396.1:n.*1742A>G
ENST00000697686.1:c.816A>G ENSP00000513397.1:p.Ile272Met
ENST00000697689.1:c.*1459A>G ENSP00000513398.1:n.*1459A>G
ENST00000697690.1:c.*5A>G ENSP00000513399.1:n.*5A>G
ENST00000697691.1:c.*1017A>G ENSP00000513400.1:n.*1017A>G
ENST00000697692.1:c.*1057A>G ENSP00000513401.1:n.*1057A>G
ENST00000697694.1:c.694A>G ENSP00000513402.1:p.Thr232Ala
ENST00000697695.1:n.1652A>G
XM_006722001.2:c.1048A>G XP_006722064.1:p.Thr350Ala
XM_006722001.4:c.1048A>G XP_006722064.1:p.Thr350Ala
XM_006722002.2:c.984A>G XP_006722065.1:p.Ile328Met
XM_006722002.4:c.984A>G XP_006722065.1:p.Ile328Met
XM_006722004.2:c.697A>G XP_006722067.1:p.Thr233Ala
XM_006722004.3:c.697A>G XP_006722067.1:p.Thr233Ala
XM_006722005.2:c.697A>G XP_006722068.1:p.Thr233Ala
XM_006722005.3:c.697A>G XP_006722068.1:p.Thr233Ala
XM_011525092.1:c.697A>G XP_011523394.1:p.Thr233Ala
XM_011525092.2:c.697A>G XP_011523394.1:p.Thr233Ala
XM_011525093.1:c.697A>G XP_011523395.1:p.Thr233Ala
XM_011525093.2:c.697A>G XP_011523395.1:p.Thr233Ala
XM_011525094.1:c.697A>G XP_011523396.1:p.Thr233Ala
XM_011525094.2:c.697A>G XP_011523396.1:p.Thr233Ala
XM_017024914.1:c.694A>G XP_016880403.1:p.Thr232Ala
XM_017024915.1:c.694A>G XP_016880404.1:p.Thr232Ala
XM_017024916.1:c.694A>G XP_016880405.1:p.Thr232Ala
XM_017024917.1:c.694A>G XP_016880406.1:p.Thr232Ala
XM_017024918.2:c.694A>G XP_016880407.1:p.Thr232Ala
XM_017024919.1:c.633A>G XP_016880408.1:p.Ile211Met
XR_934513.1:n.1263A>G
XR_934513.3:n.1694A>G
XR_934514.1:n.1266A>G
XR_934514.3:n.1697A>G
XR_934886.1:n.149+3935T>C
XR_934886.2:n.149+3935T>C