Canonical Allele Identifier: CA2267819444
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703202G= , CM000679.2:g.58703202G= GRCh38
NC_000017.10:g.56780563G= , CM000679.1:g.56780563G= GRCh37
NC_000017.9:g.54135562G= NCBI36
NG_023199.1:g.15601G= , LRG_314:g.15601G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.227G= ENSP00000464056.2:p.Arg76=
ENST00000697677.1:n.1659G=
ENST00000697678.1:n.480G=
ENST00000697679.1:n.1652G=
ENST00000697680.1:c.*1442G= ENSP00000513392.1:n.*1442G=
ENST00000697681.1:c.*1594G= ENSP00000513393.1:n.*1594G=
ENST00000697683.1:c.*1442G= ENSP00000513395.1:n.*1442G=
ENST00000697684.1:n.638G=
ENST00000697685.1:c.*1275G= ENSP00000513396.1:n.*1275G=
ENST00000697686.1:c.227G= ENSP00000513397.1:p.Arg76=
ENST00000697687.1:n.457G=
ENST00000697688.1:n.624G=
ENST00000697689.1:c.*1114G= ENSP00000513398.1:n.*1114G=
ENST00000697690.1:c.578G= ENSP00000513399.1:p.Arg193=
ENST00000697691.1:c.*550G= ENSP00000513400.1:n.*550G=
ENST00000697692.1:c.*590G= ENSP00000513401.1:n.*590G=
ENST00000697694.1:c.227G= ENSP00000513402.1:p.Arg76=
ENST00000697695.1:n.1185G=
ENST00000337432.9:c.578G= MANE Select ENSP00000336701.4:p.Arg193=
ENST00000337432.8:c.578G= ENSP00000336701.4:p.Arg193=
ENST00000413590.5:c.216G=
ENST00000425173.5:c.374G= ENSP00000407282.1:p.Arg125=
ENST00000461271.5:c.227G= ENSP00000464056.1:p.Arg76=
ENST00000475762.5:c.*1281G= ENSP00000432421.1:n.*1281G=
ENST00000482007.5:c.*6G= ENSP00000433332.1:n.*6G=
ENST00000487525.5:c.*6G= ENSP00000431637.1:n.*6G=
ENST00000487921.5:n.490G=
ENST00000583539.5:c.578G= ENSP00000463121.1:p.Arg193=
ENST00000584617.5:c.300G=
NM_058216.2:c.578G= NP_478123.1:p.Arg193=
NR_103872.1:n.482G=
XM_006722001.2:c.578G= XP_006722064.1:p.Arg193=
XM_006722002.2:c.578G= XP_006722065.1:p.Arg193=
XM_006722004.2:c.227G= XP_006722067.1:p.Arg76=
XM_006722005.2:c.227G= XP_006722068.1:p.Arg76=
XM_011525092.1:c.227G= XP_011523394.1:p.Arg76=
XM_011525093.1:c.227G= XP_011523395.1:p.Arg76=
XM_011525094.1:c.227G= XP_011523396.1:p.Arg76=
XR_934513.1:n.651G=
XR_934514.1:n.651G=
XM_006722001.4:c.578G= XP_006722064.1:p.Arg193=
XM_006722002.4:c.578G= XP_006722065.1:p.Arg193=
XM_006722004.3:c.227G= XP_006722067.1:p.Arg76=
XM_006722005.3:c.227G= XP_006722068.1:p.Arg76=
XM_011525092.2:c.227G= XP_011523394.1:p.Arg76=
XM_011525093.2:c.227G= XP_011523395.1:p.Arg76=
XM_011525094.2:c.227G= XP_011523396.1:p.Arg76=
XM_017024914.1:c.227G= XP_016880403.1:p.Arg76=
XM_017024915.1:c.227G= XP_016880404.1:p.Arg76=
XM_017024916.1:c.227G= XP_016880405.1:p.Arg76=
XM_017024917.1:c.227G= XP_016880406.1:p.Arg76=
XM_017024918.2:c.227G= XP_016880407.1:p.Arg76=
XM_017024919.1:c.227G= XP_016880408.1:p.Arg76=
XR_934513.3:n.1082G=
XR_934514.3:n.1082G=
NM_058216.3:c.578G= MANE Select NP_478123.1:p.Arg193=
NR_103872.2:n.453G=