Canonical Allele Identifier: CA400366345
Community Standard Title: NM_058216.3(RAD51C):c.1085C>T (p.Ser362Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734176C>T , CM000679.2:g.58734176C>T GRCh38
NC_000017.10:g.56811537C>T , CM000679.1:g.56811537C>T GRCh37
NC_000017.9:g.54166536C>T NCBI36
NG_023199.1:g.46575C>T , LRG_314:g.46575C>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1085C>T MANE Select NP_478123.1:p.Ser362Phe
ENST00000337432.9:c.1085C>T MANE Select ENSP00000336701.4:p.Ser362Phe
NM_058216.2:c.1085C>T NP_478123.1:p.Ser362Phe
NR_103872.1:n.989C>T
NR_103872.2:n.960C>T
ENST00000337432.8:c.1085C>T ENSP00000336701.4:p.Ser362Phe
ENST00000413590.5:c.726C>T
ENST00000461271.6:c.*1617C>T ENSP00000464056.2:n.*1617C>T
ENST00000461706.1:n.272C>T
ENST00000475762.5:c.*1721C>T ENSP00000432421.1:n.*1721C>T
ENST00000482007.5:c.*513C>T ENSP00000433332.1:n.*513C>T
ENST00000487525.5:c.*661C>T ENSP00000431637.1:n.*661C>T
ENST00000578151.1:n.298C>T
ENST00000581221.5:n.600C>T
ENST00000584804.1:c.319C>T ENSP00000463658.1:p.Pro107Ser
ENST00000697680.1:c.*2049C>T ENSP00000513392.1:n.*2049C>T
ENST00000697681.1:c.*2246C>T ENSP00000513393.1:n.*2246C>T
ENST00000697683.1:c.*2021C>T ENSP00000513395.1:n.*2021C>T
ENST00000697685.1:c.*1782C>T ENSP00000513396.1:n.*1782C>T
ENST00000697686.1:c.856C>T ENSP00000513397.1:p.Pro286Ser
ENST00000697689.1:c.*1499C>T ENSP00000513398.1:n.*1499C>T
ENST00000697690.1:c.*45C>T ENSP00000513399.1:n.*45C>T
ENST00000697691.1:c.*1057C>T ENSP00000513400.1:n.*1057C>T
ENST00000697692.1:c.*1097C>T ENSP00000513401.1:n.*1097C>T
ENST00000697694.1:c.734C>T ENSP00000513402.1:p.Ser245Phe
ENST00000697695.1:n.1692C>T
XM_006722001.2:c.1088C>T XP_006722064.1:p.Ser363Phe
XM_006722001.4:c.1088C>T XP_006722064.1:p.Ser363Phe
XM_006722002.2:c.1024C>T XP_006722065.1:p.Pro342Ser
XM_006722002.4:c.1024C>T XP_006722065.1:p.Pro342Ser
XM_006722004.2:c.737C>T XP_006722067.1:p.Ser246Phe
XM_006722004.3:c.737C>T XP_006722067.1:p.Ser246Phe
XM_006722005.2:c.737C>T XP_006722068.1:p.Ser246Phe
XM_006722005.3:c.737C>T XP_006722068.1:p.Ser246Phe
XM_011525092.1:c.737C>T XP_011523394.1:p.Ser246Phe
XM_011525092.2:c.737C>T XP_011523394.1:p.Ser246Phe
XM_011525093.1:c.737C>T XP_011523395.1:p.Ser246Phe
XM_011525093.2:c.737C>T XP_011523395.1:p.Ser246Phe
XM_011525094.1:c.737C>T XP_011523396.1:p.Ser246Phe
XM_011525094.2:c.737C>T XP_011523396.1:p.Ser246Phe
XM_017024914.1:c.734C>T XP_016880403.1:p.Ser245Phe
XM_017024915.1:c.734C>T XP_016880404.1:p.Ser245Phe
XM_017024916.1:c.734C>T XP_016880405.1:p.Ser245Phe
XM_017024917.1:c.734C>T XP_016880406.1:p.Ser245Phe
XM_017024918.2:c.734C>T XP_016880407.1:p.Ser245Phe
XM_017024919.1:c.673C>T XP_016880408.1:p.Pro225Ser
XR_934513.1:n.1303C>T
XR_934513.3:n.1734C>T
XR_934514.1:n.1306C>T
XR_934514.3:n.1737C>T
XR_934886.1:n.149+3895G>A
XR_934886.2:n.149+3895G>A