Canonical Allele Identifier: CA2267815308
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695080T= , CM000679.2:g.58695080T= GRCh38
NC_000017.10:g.56772441T= , CM000679.1:g.56772441T= GRCh37
NC_000017.9:g.54127440T= NCBI36
NG_023199.1:g.7479T= , LRG_314:g.7479T=
NG_047169.1:g.2000A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-57T= ENSP00000464056.2:n.-57T=
ENST00000697675.1:n.1389T=
ENST00000697676.1:n.355T=
ENST00000697677.1:n.1376T=
ENST00000697678.1:n.197T=
ENST00000697679.1:n.1369T=
ENST00000697680.1:c.*1159T= ENSP00000513392.1:n.*1159T=
ENST00000697681.1:c.*1159T= ENSP00000513393.1:n.*1159T=
ENST00000697683.1:c.*1159T= ENSP00000513395.1:n.*1159T=
ENST00000697684.1:n.355T=
ENST00000697685.1:c.*1159T= ENSP00000513396.1:n.*1159T=
ENST00000697686.1:c.-57T= ENSP00000513397.1:n.-57T=
ENST00000697687.1:n.341T=
ENST00000697688.1:n.341T=
ENST00000697689.1:c.*998T= ENSP00000513398.1:n.*998T=
ENST00000697690.1:c.295T= ENSP00000513399.1:p.Phe99=
ENST00000697691.1:c.*267T= ENSP00000513400.1:n.*267T=
ENST00000697692.1:c.*307T= ENSP00000513401.1:n.*307T=
ENST00000697693.1:n.1070T=
ENST00000697694.1:c.-57T= ENSP00000513402.1:n.-57T=
ENST00000697695.1:n.902T=
ENST00000337432.9:c.295T= MANE Select ENSP00000336701.4:p.Phe99=
ENST00000337432.8:c.295T= ENSP00000336701.4:p.Phe99=
ENST00000421782.3:c.295T= ENSP00000391450.2:p.Phe99=
ENST00000425173.5:c.91T= ENSP00000407282.1:p.Phe31=
ENST00000461271.5:c.-57T= ENSP00000464056.1:n.-57T=
ENST00000475762.5:c.*998T= ENSP00000432421.1:n.*998T=
ENST00000482007.5:c.295T= ENSP00000433332.1:p.Phe99=
ENST00000486827.1:c.*1159T= ENSP00000436761.1:n.*1159T=
ENST00000487525.5:c.295T= ENSP00000431637.1:p.Phe99=
ENST00000487921.5:n.207T=
ENST00000583539.5:c.295T= ENSP00000463121.1:p.Phe99=
ENST00000584617.5:c.127-1613T=
ENST00000622327.4:c.31T= ENSP00000482326.1:p.Phe11=
NM_002876.3:c.295T= NP_002867.1:p.Phe99=
NM_058216.2:c.295T= NP_478123.1:p.Phe99=
NR_103872.1:n.366T=
NR_103873.1:n.263T=
XM_006722001.2:c.295T= XP_006722064.1:p.Phe99=
XM_006722002.2:c.295T= XP_006722065.1:p.Phe99=
XM_006722004.2:c.-57T= XP_006722067.1:n.-57T=
XM_006722005.2:c.-57T= XP_006722068.1:n.-57T=
XM_011525092.1:c.-57T= XP_011523394.1:n.-57T=
XM_011525093.1:c.-57T= XP_011523395.1:n.-57T=
XM_011525094.1:c.-57T= XP_011523396.1:n.-57T=
XR_934513.1:n.368T=
XR_934514.1:n.368T=
XM_006722001.4:c.295T= XP_006722064.1:p.Phe99=
XM_006722002.4:c.295T= XP_006722065.1:p.Phe99=
XM_006722004.3:c.-57T= XP_006722067.1:n.-57T=
XM_006722005.3:c.-57T= XP_006722068.1:n.-57T=
XM_011525092.2:c.-57T= XP_011523394.1:n.-57T=
XM_011525093.2:c.-57T= XP_011523395.1:n.-57T=
XM_011525094.2:c.-57T= XP_011523396.1:n.-57T=
XM_017024914.1:c.-57T= XP_016880403.1:n.-57T=
XM_017024915.1:c.-57T= XP_016880404.1:n.-57T=
XM_017024916.1:c.-57T= XP_016880405.1:n.-57T=
XM_017024917.1:c.-57T= XP_016880406.1:n.-57T=
XM_017024918.2:c.-57T= XP_016880407.1:n.-57T=
XM_017024919.1:c.-57T= XP_016880408.1:n.-57T=
XR_934513.3:n.799T=
XR_934514.3:n.799T=
NM_058216.3:c.295T= MANE Select NP_478123.1:p.Phe99=
NR_103872.2:n.337T=
NM_002876.4:c.295T= NP_002867.1:p.Phe99=