Canonical Allele Identifier: CA2267829099
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724069C= , CM000679.2:g.58724069C= GRCh38
NC_000017.10:g.56801430C= , CM000679.1:g.56801430C= GRCh37
NC_000017.9:g.54156429C= NCBI36
NG_023199.1:g.36468C= , LRG_314:g.36468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.583C= ENSP00000464056.2:p.Arg195=
ENST00000697680.1:c.*1898C= ENSP00000513392.1:n.*1898C=
ENST00000697681.1:c.*2095C= ENSP00000513393.1:n.*2095C=
ENST00000697683.1:c.*1798C= ENSP00000513395.1:n.*1798C=
ENST00000697684.1:n.994C=
ENST00000697685.1:c.*1631C= ENSP00000513396.1:n.*1631C=
ENST00000697686.1:c.583C= ENSP00000513397.1:p.Arg195=
ENST00000697687.1:n.813C=
ENST00000697688.1:n.980C=
ENST00000697689.1:c.*1440+3257C= ENSP00000513398.1:n.*1440+3257C=
ENST00000697690.1:c.904+3257C= ENSP00000513399.1:n.904+3257C=
ENST00000697691.1:c.*906C= ENSP00000513400.1:n.*906C=
ENST00000697692.1:c.*946C= ENSP00000513401.1:n.*946C=
ENST00000697694.1:c.583C= ENSP00000513402.1:p.Arg195=
ENST00000697695.1:n.1541C=
ENST00000337432.9:c.934C= MANE Select ENSP00000336701.4:p.Arg312=
ENST00000337432.8:c.934C= ENSP00000336701.4:p.Arg312=
ENST00000413590.5:c.572C=
ENST00000475762.5:c.*1570C= ENSP00000432421.1:n.*1570C=
ENST00000482007.5:c.*362C= ENSP00000433332.1:n.*362C=
ENST00000487525.5:c.*507C= ENSP00000431637.1:n.*507C=
ENST00000578151.1:n.239+3257C=
ENST00000581221.5:n.449C=
ENST00000583539.5:c.934C= ENSP00000463121.1:p.Arg312=
ENST00000584617.5:c.656C=
ENST00000584804.1:c.199+3257C= ENSP00000463658.1:n.199+3257C=
NM_058216.2:c.934C= NP_478123.1:p.Arg312=
NR_103872.1:n.838C=
XM_006722001.2:c.934C= XP_006722064.1:p.Arg312=
XM_006722002.2:c.904+3257C= XP_006722065.1:n.904+3257C=
XM_006722004.2:c.583C= XP_006722067.1:p.Arg195=
XM_006722005.2:c.583C= XP_006722068.1:p.Arg195=
XM_011525092.1:c.583C= XP_011523394.1:p.Arg195=
XM_011525093.1:c.583C= XP_011523395.1:p.Arg195=
XM_011525094.1:c.583C= XP_011523396.1:p.Arg195=
XR_934513.1:n.1152C=
XR_934514.1:n.1152C=
XM_006722001.4:c.934C= XP_006722064.1:p.Arg312=
XM_006722002.4:c.904+3257C= XP_006722065.1:n.904+3257C=
XM_006722004.3:c.583C= XP_006722067.1:p.Arg195=
XM_006722005.3:c.583C= XP_006722068.1:p.Arg195=
XM_011525092.2:c.583C= XP_011523394.1:p.Arg195=
XM_011525093.2:c.583C= XP_011523395.1:p.Arg195=
XM_011525094.2:c.583C= XP_011523396.1:p.Arg195=
XM_017024914.1:c.583C= XP_016880403.1:p.Arg195=
XM_017024915.1:c.583C= XP_016880404.1:p.Arg195=
XM_017024916.1:c.583C= XP_016880405.1:p.Arg195=
XM_017024917.1:c.583C= XP_016880406.1:p.Arg195=
XM_017024918.2:c.583C= XP_016880407.1:p.Arg195=
XM_017024919.1:c.553+3257C= XP_016880408.1:n.553+3257C=
XR_934513.3:n.1583C=
XR_934514.3:n.1583C=
NM_058216.3:c.934C= MANE Select NP_478123.1:p.Arg312=
NR_103872.2:n.809C=