Canonical Allele Identifier: CA1139665725

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 959376
• ClinVar RCV Id: RCV001232717 ; RCV004033176
• dbSNP Id: rs2047953067

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695098_58695099insA , CM000679.2:g.58695098_58695099insA	GRCh38
NC_000017.10:g.56772459_56772460insA , CM000679.1:g.56772459_56772460insA	GRCh37
NC_000017.9:g.54127458_54127459insA	NCBI36
NG_023199.1:g.7497_7498insA , LRG_314:g.7497_7498insA
NG_047169.1:g.1981_1982insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-39_-38insA	ENSP00000464056.2:n.-39_-38insA
ENST00000697675.1:n.1407_1408insA
ENST00000697676.1:n.373_374insA
ENST00000697677.1:n.1394_1395insA
ENST00000697678.1:n.215_216insA
ENST00000697679.1:n.1387_1388insA
ENST00000697680.1:c.*1177_*1178insA	ENSP00000513392.1:n.*1177_*1178insA
ENST00000697681.1:c.*1177_*1178insA	ENSP00000513393.1:n.*1177_*1178insA
ENST00000697683.1:c.*1177_*1178insA	ENSP00000513395.1:n.*1177_*1178insA
ENST00000697684.1:n.373_374insA
ENST00000697685.1:c.*1177_*1178insA	ENSP00000513396.1:n.*1177_*1178insA
ENST00000697686.1:c.-39_-38insA	ENSP00000513397.1:n.-39_-38insA
ENST00000697687.1:n.359_360insA
ENST00000697688.1:n.359_360insA
ENST00000697689.1:c.*1016_*1017insA	ENSP00000513398.1:n.*1016_*1017insA
ENST00000697690.1:c.313_314insA	ENSP00000513399.1:p.Ser105TyrfsTer5
ENST00000697691.1:c.*285_*286insA	ENSP00000513400.1:n.*285_*286insA
ENST00000697692.1:c.*325_*326insA	ENSP00000513401.1:n.*325_*326insA
ENST00000697693.1:n.1088_1089insA
ENST00000697694.1:c.-39_-38insA	ENSP00000513402.1:n.-39_-38insA
ENST00000697695.1:n.920_921insA
ENST00000337432.9:c.313_314insA MANE Select	ENSP00000336701.4:p.Ser105TyrfsTer5
ENST00000337432.8:c.313_314insA	ENSP00000336701.4:p.Ser105TyrfsTer5
ENST00000421782.3:c.313_314insA	ENSP00000391450.2:p.Ser105TyrfsTer5
ENST00000425173.5:c.109_110insA	ENSP00000407282.1:p.Ser37TyrfsTer5
ENST00000461271.5:c.-39_-38insA	ENSP00000464056.1:n.-39_-38insA
ENST00000475762.5:c.*1016_*1017insA	ENSP00000432421.1:n.*1016_*1017insA
ENST00000482007.5:c.313_314insA	ENSP00000433332.1:p.Ser105TyrfsTer5
ENST00000486827.1:c.*1177_*1178insA	ENSP00000436761.1:n.*1177_*1178insA
ENST00000487525.5:c.313_314insA	ENSP00000431637.1:p.Ser105TyrfsTer5
ENST00000487921.5:n.225_226insA
ENST00000583539.5:c.313_314insA	ENSP00000463121.1:p.Ser105TyrfsTer5
ENST00000584617.5:c.127-1595_127-1594insA
ENST00000622327.4:c.49_50insA	ENSP00000482326.1:p.Ser17TyrfsTer5
NM_002876.3:c.313_314insA	NP_002867.1:p.Ser105TyrfsTer5
NM_058216.2:c.313_314insA	NP_478123.1:p.Ser105TyrfsTer5
NR_103872.1:n.384_385insA
NR_103873.1:n.281_282insA
XM_006722001.2:c.313_314insA	XP_006722064.1:p.Ser105TyrfsTer5
XM_006722002.2:c.313_314insA	XP_006722065.1:p.Ser105TyrfsTer5
XM_006722004.2:c.-39_-38insA	XP_006722067.1:n.-39_-38insA
XM_006722005.2:c.-39_-38insA	XP_006722068.1:n.-39_-38insA
XM_011525092.1:c.-39_-38insA	XP_011523394.1:n.-39_-38insA
XM_011525093.1:c.-39_-38insA	XP_011523395.1:n.-39_-38insA
XM_011525094.1:c.-39_-38insA	XP_011523396.1:n.-39_-38insA
XR_934513.1:n.386_387insA
XR_934514.1:n.386_387insA
XM_006722001.4:c.313_314insA	XP_006722064.1:p.Ser105TyrfsTer5
XM_006722002.4:c.313_314insA	XP_006722065.1:p.Ser105TyrfsTer5
XM_006722004.3:c.-39_-38insA	XP_006722067.1:n.-39_-38insA
XM_006722005.3:c.-39_-38insA	XP_006722068.1:n.-39_-38insA
XM_011525092.2:c.-39_-38insA	XP_011523394.1:n.-39_-38insA
XM_011525093.2:c.-39_-38insA	XP_011523395.1:n.-39_-38insA
XM_011525094.2:c.-39_-38insA	XP_011523396.1:n.-39_-38insA
XM_017024914.1:c.-39_-38insA	XP_016880403.1:n.-39_-38insA
XM_017024915.1:c.-39_-38insA	XP_016880404.1:n.-39_-38insA
XM_017024916.1:c.-39_-38insA	XP_016880405.1:n.-39_-38insA
XM_017024917.1:c.-39_-38insA	XP_016880406.1:n.-39_-38insA
XM_017024918.2:c.-39_-38insA	XP_016880407.1:n.-39_-38insA
XM_017024919.1:c.-39_-38insA	XP_016880408.1:n.-39_-38insA
XR_934513.3:n.817_818insA
XR_934514.3:n.817_818insA
NM_058216.3:c.313_314insA MANE Select	NP_478123.1:p.Ser105TyrfsTer5
NR_103872.2:n.355_356insA
NM_002876.4:c.313_314insA	NP_002867.1:p.Ser105TyrfsTer5