Canonical Allele Identifier: CA2638988986
Gene: RAD51C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692986_58692987insCCACAAAAGTT , CM000679.2:g.58692986_58692987insCCACAAAAGTT GRCh38
NC_000017.10:g.56770347_56770348insCCACAAAAGTT , CM000679.1:g.56770347_56770348insCCACAAAAGTT GRCh37
NC_000017.9:g.54125346_54125347insCCACAAAAGTT NCBI36
NG_023199.1:g.5385_5386insCCACAAAAGTT , LRG_314:g.5385_5386insCCACAAAAGTT
NG_047169.1:g.4093_4094insAACTTTTGTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-207+301_-207+302insCCACAAAAGTT ENSP00000464056.2:n.-207+301_-207+302insCCACAAAAGTT
ENST00000697675.1:n.414_415insCCACAAAAGTT
ENST00000697676.1:n.205+198_205+199insCCACAAAAGTT
ENST00000697677.1:n.401_402insCCACAAAAGTT
ENST00000697678.1:n.47+354_47+355insCCACAAAAGTT
ENST00000697679.1:n.394_395insCCACAAAAGTT
ENST00000697680.1:c.*184_*185insCCACAAAAGTT ENSP00000513392.1:n.*184_*185insCCACAAAAGTT
ENST00000697681.1:c.*184_*185insCCACAAAAGTT ENSP00000513393.1:n.*184_*185insCCACAAAAGTT
ENST00000697683.1:c.*184_*185insCCACAAAAGTT ENSP00000513395.1:n.*184_*185insCCACAAAAGTT
ENST00000697684.1:n.205+198_205+199insCCACAAAAGTT
ENST00000697685.1:c.*184_*185insCCACAAAAGTT ENSP00000513396.1:n.*184_*185insCCACAAAAGTT
ENST00000697686.1:c.-207+354_-207+355insCCACAAAAGTT ENSP00000513397.1:n.-207+354_-207+355insCCACAAAAGTT
ENST00000697687.1:n.191+198_191+199insCCACAAAAGTT
ENST00000697688.1:n.191+198_191+199insCCACAAAAGTT
ENST00000697689.1:c.*184_*185insCCACAAAAGTT ENSP00000513398.1:n.*184_*185insCCACAAAAGTT
ENST00000697690.1:c.145+198_145+199insCCACAAAAGTT ENSP00000513399.1:n.145+198_145+199insCCACAAAAGTT
ENST00000697691.1:c.42+301_42+302insCCACAAAAGTT ENSP00000513400.1:n.42+301_42+302insCCACAAAAGTT
ENST00000697692.1:c.*157+27_*157+28insCCACAAAAGTT ENSP00000513401.1:n.*157+27_*157+28insCCACAAAAGTT
ENST00000697693.1:n.256_257insCCACAAAAGTT
ENST00000697694.1:c.-339_-338insCCACAAAAGTT ENSP00000513402.1:n.-339_-338insCCACAAAAGTT
ENST00000697695.1:n.60_61insCCACAAAAGTT
ENST00000337432.9:c.145+198_145+199insCCACAAAAGTT MANE Select ENSP00000336701.4:n.145+198_145+199insCCACAAAAGTT
ENST00000337432.8:c.145+198_145+199insCCACAAAAGTT ENSP00000336701.4:n.145+198_145+199insCCACAAAAGTT
ENST00000421782.3:c.145+198_145+199insCCACAAAAGTT ENSP00000391450.2:n.145+198_145+199insCCACAAAAGTT
ENST00000461271.5:c.-207+301_-207+302insCCACAAAAGTT ENSP00000464056.1:n.-207+301_-207+302insCCACAAAAGTT
ENST00000475762.5:c.*184_*185insCCACAAAAGTT ENSP00000432421.1:n.*184_*185insCCACAAAAGTT
ENST00000476741.2:n.187+198_187+199insCCACAAAAGTT
ENST00000482007.5:c.145+198_145+199insCCACAAAAGTT ENSP00000433332.1:n.145+198_145+199insCCACAAAAGTT
ENST00000486827.1:c.*184_*185insCCACAAAAGTT ENSP00000436761.1:n.*184_*185insCCACAAAAGTT
ENST00000487525.5:c.145+198_145+199insCCACAAAAGTT ENSP00000431637.1:n.145+198_145+199insCCACAAAAGTT
ENST00000487921.5:n.57+354_57+355insCCACAAAAGTT
ENST00000583539.5:c.145+198_145+199insCCACAAAAGTT ENSP00000463121.1:n.145+198_145+199insCCACAAAAGTT
ENST00000584617.5:c.126+198_126+199insCCACAAAAGTT
NM_002876.3:c.145+198_145+199insCCACAAAAGTT NP_002867.1:n.145+198_145+199insCCACAAAAGTT
NM_058216.2:c.145+198_145+199insCCACAAAAGTT NP_478123.1:n.145+198_145+199insCCACAAAAGTT
NR_103872.1:n.216+198_216+199insCCACAAAAGTT
NR_103873.1:n.113+301_113+302insCCACAAAAGTT
XM_006722001.2:c.145+198_145+199insCCACAAAAGTT XP_006722064.1:n.145+198_145+199insCCACAAAAGTT
XM_006722002.2:c.145+198_145+199insCCACAAAAGTT XP_006722065.1:n.145+198_145+199insCCACAAAAGTT
XM_006722004.2:c.-207+301_-207+302insCCACAAAAGTT XP_006722067.1:n.-207+301_-207+302insCCACAAAAGTT
XM_006722005.2:c.-207+354_-207+355insCCACAAAAGTT XP_006722068.1:n.-207+354_-207+355insCCACAAAAGTT
XM_011525092.1:c.-507+301_-507+302insCCACAAAAGTT XP_011523394.1:n.-507+301_-507+302insCCACAAAAGTT
XM_011525093.1:c.-668+301_-668+302insCCACAAAAGTT XP_011523395.1:n.-668+301_-668+302insCCACAAAAGTT
XM_011525094.1:c.-207+27_-207+28insCCACAAAAGTT XP_011523396.1:n.-207+27_-207+28insCCACAAAAGTT
XR_934513.1:n.218+198_218+199insCCACAAAAGTT
XR_934514.1:n.218+198_218+199insCCACAAAAGTT
XM_006722001.4:c.145+198_145+199insCCACAAAAGTT XP_006722064.1:n.145+198_145+199insCCACAAAAGTT
XM_006722002.4:c.145+198_145+199insCCACAAAAGTT XP_006722065.1:n.145+198_145+199insCCACAAAAGTT
XM_006722004.3:c.-207+301_-207+302insCCACAAAAGTT XP_006722067.1:n.-207+301_-207+302insCCACAAAAGTT
XM_006722005.3:c.-207+354_-207+355insCCACAAAAGTT XP_006722068.1:n.-207+354_-207+355insCCACAAAAGTT
XM_011525092.2:c.-507+301_-507+302insCCACAAAAGTT XP_011523394.1:n.-507+301_-507+302insCCACAAAAGTT
XM_011525093.2:c.-668+301_-668+302insCCACAAAAGTT XP_011523395.1:n.-668+301_-668+302insCCACAAAAGTT
XM_011525094.2:c.-207+27_-207+28insCCACAAAAGTT XP_011523396.1:n.-207+27_-207+28insCCACAAAAGTT
XM_017024914.1:c.-207+301_-207+302insCCACAAAAGTT XP_016880403.1:n.-207+301_-207+302insCCACAAAAGTT
XM_017024916.1:c.-507+301_-507+302insCCACAAAAGTT XP_016880405.1:n.-507+301_-507+302insCCACAAAAGTT
XM_017024917.1:c.-207+354_-207+355insCCACAAAAGTT XP_016880406.1:n.-207+354_-207+355insCCACAAAAGTT
XM_017024918.2:c.-207+27_-207+28insCCACAAAAGTT XP_016880407.1:n.-207+27_-207+28insCCACAAAAGTT
XM_017024919.1:c.-668+301_-668+302insCCACAAAAGTT XP_016880408.1:n.-668+301_-668+302insCCACAAAAGTT
XR_934513.3:n.649+198_649+199insCCACAAAAGTT
XR_934514.3:n.649+198_649+199insCCACAAAAGTT
NM_058216.3:c.145+198_145+199insCCACAAAAGTT MANE Select NP_478123.1:n.145+198_145+199insCCACAAAAGTT
NR_103872.2:n.187+198_187+199insCCACAAAAGTT
NM_002876.4:c.145+198_145+199insCCACAAAAGTT NP_002867.1:n.145+198_145+199insCCACAAAAGTT