Canonical Allele Identifier: CA3057243452
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732523_58732524delinsTT , CM000679.2:g.58732523_58732524delinsTT GRCh38
NC_000017.10:g.56809884_56809885delinsTT , CM000679.1:g.56809884_56809885delinsTT GRCh37
NC_000017.9:g.54164883_54164884delinsTT NCBI36
NG_023199.1:g.44922_44923delinsTT , LRG_314:g.44922_44923delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.654_655delinsTT ENSP00000464056.2:p.Thr219Ser
ENST00000697680.1:c.*1969_*1970delinsTT ENSP00000513392.1:n.*1969_*1970delinsTT
ENST00000697681.1:c.*2166_*2167delinsTT ENSP00000513393.1:n.*2166_*2167delinsTT
ENST00000697683.1:c.*1941_*1942delinsTT ENSP00000513395.1:n.*1941_*1942delinsTT
ENST00000697685.1:c.*1702_*1703delinsTT ENSP00000513396.1:n.*1702_*1703delinsTT
ENST00000697686.1:c.776_777delinsTT ENSP00000513397.1:p.Ala259Val
ENST00000697689.1:c.*1441-1595_*1441-1594delinsTT ENSP00000513398.1:n.*1441-1595_*1441-1594delinsTT
ENST00000697690.1:c.905-1595_905-1594delinsTT ENSP00000513399.1:n.905-1595_905-1594delinsTT
ENST00000697691.1:c.*977_*978delinsTT ENSP00000513400.1:n.*977_*978delinsTT
ENST00000697692.1:c.*1017_*1018delinsTT ENSP00000513401.1:n.*1017_*1018delinsTT
ENST00000697694.1:c.654_655delinsTT ENSP00000513402.1:p.Thr219Ser
ENST00000697695.1:n.1612_1613delinsTT
ENST00000337432.9:c.1005_1006delinsTT MANE Select ENSP00000336701.4:p.Thr336Ser
ENST00000337432.8:c.1005_1006delinsTT ENSP00000336701.4:p.Thr336Ser
ENST00000413590.5:c.646_647delinsTT
ENST00000461706.1:n.192_193delinsTT
ENST00000475762.5:c.*1641_*1642delinsTT ENSP00000432421.1:n.*1641_*1642delinsTT
ENST00000482007.5:c.*433_*434delinsTT ENSP00000433332.1:n.*433_*434delinsTT
ENST00000487525.5:c.*581_*582delinsTT ENSP00000431637.1:n.*581_*582delinsTT
ENST00000578151.1:n.240-1595_240-1594delinsTT
ENST00000581221.5:n.520_521delinsTT
ENST00000583539.5:c.1005_1006delinsTT ENSP00000463121.1:p.Thr336Ser
ENST00000584804.1:c.239_240delinsTT ENSP00000463658.1:p.Ala80Val
NM_058216.2:c.1005_1006delinsTT NP_478123.1:p.Thr336Ser
NR_103872.1:n.909_910delinsTT
XM_006722001.2:c.1008_1009delinsTT XP_006722064.1:p.Thr337Ser
XM_006722002.2:c.944_945delinsTT XP_006722065.1:p.Ala315Val
XM_006722004.2:c.657_658delinsTT XP_006722067.1:p.Thr220Ser
XM_006722005.2:c.657_658delinsTT XP_006722068.1:p.Thr220Ser
XM_011525092.1:c.657_658delinsTT XP_011523394.1:p.Thr220Ser
XM_011525093.1:c.657_658delinsTT XP_011523395.1:p.Thr220Ser
XM_011525094.1:c.657_658delinsTT XP_011523396.1:p.Thr220Ser
XR_934513.1:n.1223_1224delinsTT
XR_934514.1:n.1226_1227delinsTT
XR_934886.1:n.149+5547_149+5548delinsAA
XM_006722001.4:c.1008_1009delinsTT XP_006722064.1:p.Thr337Ser
XM_006722002.4:c.944_945delinsTT XP_006722065.1:p.Ala315Val
XM_006722004.3:c.657_658delinsTT XP_006722067.1:p.Thr220Ser
XM_006722005.3:c.657_658delinsTT XP_006722068.1:p.Thr220Ser
XM_011525092.2:c.657_658delinsTT XP_011523394.1:p.Thr220Ser
XM_011525093.2:c.657_658delinsTT XP_011523395.1:p.Thr220Ser
XM_011525094.2:c.657_658delinsTT XP_011523396.1:p.Thr220Ser
XM_017024914.1:c.654_655delinsTT XP_016880403.1:p.Thr219Ser
XM_017024915.1:c.654_655delinsTT XP_016880404.1:p.Thr219Ser
XM_017024916.1:c.654_655delinsTT XP_016880405.1:p.Thr219Ser
XM_017024917.1:c.654_655delinsTT XP_016880406.1:p.Thr219Ser
XM_017024918.2:c.654_655delinsTT XP_016880407.1:p.Thr219Ser
XM_017024919.1:c.593_594delinsTT XP_016880408.1:p.Ala198Val
XR_934513.3:n.1654_1655delinsTT
XR_934514.3:n.1657_1658delinsTT
XR_934886.2:n.149+5547_149+5548delinsAA
NM_058216.3:c.1005_1006delinsTT MANE Select NP_478123.1:p.Thr336Ser
NR_103872.2:n.880_881delinsTT