Canonical Allele Identifier: CA2267822518
Community Standard Title: NM_058216.3(RAD51C):c.774T= (p.Arg258=)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709927T= , CM000679.2:g.58709927T= GRCh38
NC_000017.10:g.56787288T= , CM000679.1:g.56787288T= GRCh37
NC_000017.9:g.54142287T= NCBI36
NG_023199.1:g.22326T= , LRG_314:g.22326T=

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.774T= MANE Select NP_478123.1:p.Arg258=
ENST00000337432.9:c.774T= MANE Select ENSP00000336701.4:p.Arg258=
NM_058216.2:c.774T= NP_478123.1:p.Arg258=
NR_103872.1:n.678T=
NR_103872.2:n.649T=
ENST00000337432.8:c.774T= ENSP00000336701.4:p.Arg258=
ENST00000413590.5:c.412T=
ENST00000461271.6:c.423T= ENSP00000464056.2:p.Arg141=
ENST00000475762.5:c.*1477T= ENSP00000432421.1:n.*1477T=
ENST00000482007.5:c.*202T= ENSP00000433332.1:n.*202T=
ENST00000487525.5:c.*347T= ENSP00000431637.1:n.*347T=
ENST00000578151.1:n.109T=
ENST00000581221.5:n.289T=
ENST00000583539.5:c.774T= ENSP00000463121.1:p.Arg258=
ENST00000584617.5:c.496T=
ENST00000584804.1:c.69T= ENSP00000463658.1:p.Arg23=
ENST00000697678.1:n.676T=
ENST00000697679.1:n.1848T=
ENST00000697680.1:c.*1638T= ENSP00000513392.1:n.*1638T=
ENST00000697681.1:c.*1935T= ENSP00000513393.1:n.*1935T=
ENST00000697683.1:c.*1638T= ENSP00000513395.1:n.*1638T=
ENST00000697684.1:n.834T=
ENST00000697685.1:c.*1471T= ENSP00000513396.1:n.*1471T=
ENST00000697686.1:c.423T= ENSP00000513397.1:p.Arg141=
ENST00000697687.1:n.653T=
ENST00000697688.1:n.820T=
ENST00000697689.1:c.*1310T= ENSP00000513398.1:n.*1310T=
ENST00000697690.1:c.774T= ENSP00000513399.1:p.Arg258=
ENST00000697691.1:c.*746T= ENSP00000513400.1:n.*746T=
ENST00000697692.1:c.*786T= ENSP00000513401.1:n.*786T=
ENST00000697694.1:c.423T= ENSP00000513402.1:p.Arg141=
ENST00000697695.1:n.1381T=
XM_006722001.2:c.774T= XP_006722064.1:p.Arg258=
XM_006722001.4:c.774T= XP_006722064.1:p.Arg258=
XM_006722002.2:c.774T= XP_006722065.1:p.Arg258=
XM_006722002.4:c.774T= XP_006722065.1:p.Arg258=
XM_006722004.2:c.423T= XP_006722067.1:p.Arg141=
XM_006722004.3:c.423T= XP_006722067.1:p.Arg141=
XM_006722005.2:c.423T= XP_006722068.1:p.Arg141=
XM_006722005.3:c.423T= XP_006722068.1:p.Arg141=
XM_011525092.1:c.423T= XP_011523394.1:p.Arg141=
XM_011525092.2:c.423T= XP_011523394.1:p.Arg141=
XM_011525093.1:c.423T= XP_011523395.1:p.Arg141=
XM_011525093.2:c.423T= XP_011523395.1:p.Arg141=
XM_011525094.1:c.423T= XP_011523396.1:p.Arg141=
XM_011525094.2:c.423T= XP_011523396.1:p.Arg141=
XM_017024914.1:c.423T= XP_016880403.1:p.Arg141=
XM_017024915.1:c.423T= XP_016880404.1:p.Arg141=
XM_017024916.1:c.423T= XP_016880405.1:p.Arg141=
XM_017024917.1:c.423T= XP_016880406.1:p.Arg141=
XM_017024918.2:c.423T= XP_016880407.1:p.Arg141=
XM_017024919.1:c.423T= XP_016880408.1:p.Arg141=
XR_934513.1:n.992T=
XR_934513.3:n.1423T=
XR_934514.1:n.992T=
XR_934514.3:n.1423T=