Canonical Allele Identifier: CA3261179898
Community Standard Title: NM_058216.3(RAD51C):c.1046_1047delinsTC (p.Thr349Ile)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734137_58734138delinsTC , CM000679.2:g.58734137_58734138delinsTC GRCh38
NC_000017.10:g.56811498_56811499delinsTC , CM000679.1:g.56811498_56811499delinsTC GRCh37
NC_000017.9:g.54166497_54166498delinsTC NCBI36
NG_023199.1:g.46536_46537delinsTC , LRG_314:g.46536_46537delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1046_1047delinsTC MANE Select NP_478123.1:p.Thr349Ile
ENST00000337432.9:c.1046_1047delinsTC MANE Select ENSP00000336701.4:p.Thr349Ile
NM_058216.2:c.1046_1047delinsTC NP_478123.1:p.Thr349Ile
NR_103872.1:n.950_951delinsTC
NR_103872.2:n.921_922delinsTC
ENST00000337432.8:c.1046_1047delinsTC ENSP00000336701.4:p.Thr349Ile
ENST00000413590.5:c.687_688delinsTC
ENST00000461271.6:c.*1578_*1579delinsTC ENSP00000464056.2:n.*1578_*1579delinsTC
ENST00000461706.1:n.233_234delinsTC
ENST00000475762.5:c.*1682_*1683delinsTC ENSP00000432421.1:n.*1682_*1683delinsTC
ENST00000482007.5:c.*474_*475delinsTC ENSP00000433332.1:n.*474_*475delinsTC
ENST00000487525.5:c.*622_*623delinsTC ENSP00000431637.1:n.*622_*623delinsTC
ENST00000578151.1:n.259_260delinsTC
ENST00000581221.5:n.561_562delinsTC
ENST00000584804.1:c.280_281delinsTC ENSP00000463658.1:p.Leu94Ser
ENST00000697680.1:c.*2010_*2011delinsTC ENSP00000513392.1:n.*2010_*2011delinsTC
ENST00000697681.1:c.*2207_*2208delinsTC ENSP00000513393.1:n.*2207_*2208delinsTC
ENST00000697683.1:c.*1982_*1983delinsTC ENSP00000513395.1:n.*1982_*1983delinsTC
ENST00000697685.1:c.*1743_*1744delinsTC ENSP00000513396.1:n.*1743_*1744delinsTC
ENST00000697686.1:c.817_818delinsTC ENSP00000513397.1:p.Leu273Ser
ENST00000697689.1:c.*1460_*1461delinsTC ENSP00000513398.1:n.*1460_*1461delinsTC
ENST00000697690.1:c.*6_*7delinsTC ENSP00000513399.1:n.*6_*7delinsTC
ENST00000697691.1:c.*1018_*1019delinsTC ENSP00000513400.1:n.*1018_*1019delinsTC
ENST00000697692.1:c.*1058_*1059delinsTC ENSP00000513401.1:n.*1058_*1059delinsTC
ENST00000697694.1:c.695_696delinsTC ENSP00000513402.1:p.Thr232Ile
ENST00000697695.1:n.1653_1654delinsTC
XM_006722001.2:c.1049_1050delinsTC XP_006722064.1:p.Thr350Ile
XM_006722001.4:c.1049_1050delinsTC XP_006722064.1:p.Thr350Ile
XM_006722002.2:c.985_986delinsTC XP_006722065.1:p.Leu329Ser
XM_006722002.4:c.985_986delinsTC XP_006722065.1:p.Leu329Ser
XM_006722004.2:c.698_699delinsTC XP_006722067.1:p.Thr233Ile
XM_006722004.3:c.698_699delinsTC XP_006722067.1:p.Thr233Ile
XM_006722005.2:c.698_699delinsTC XP_006722068.1:p.Thr233Ile
XM_006722005.3:c.698_699delinsTC XP_006722068.1:p.Thr233Ile
XM_011525092.1:c.698_699delinsTC XP_011523394.1:p.Thr233Ile
XM_011525092.2:c.698_699delinsTC XP_011523394.1:p.Thr233Ile
XM_011525093.1:c.698_699delinsTC XP_011523395.1:p.Thr233Ile
XM_011525093.2:c.698_699delinsTC XP_011523395.1:p.Thr233Ile
XM_011525094.1:c.698_699delinsTC XP_011523396.1:p.Thr233Ile
XM_011525094.2:c.698_699delinsTC XP_011523396.1:p.Thr233Ile
XM_017024914.1:c.695_696delinsTC XP_016880403.1:p.Thr232Ile
XM_017024915.1:c.695_696delinsTC XP_016880404.1:p.Thr232Ile
XM_017024916.1:c.695_696delinsTC XP_016880405.1:p.Thr232Ile
XM_017024917.1:c.695_696delinsTC XP_016880406.1:p.Thr232Ile
XM_017024918.2:c.695_696delinsTC XP_016880407.1:p.Thr232Ile
XM_017024919.1:c.634_635delinsTC XP_016880408.1:p.Leu212Ser
XR_934513.1:n.1264_1265delinsTC
XR_934513.3:n.1695_1696delinsTC
XR_934514.1:n.1267_1268delinsTC
XR_934514.3:n.1698_1699delinsTC
XR_934886.1:n.149+3933_149+3934delinsGA
XR_934886.2:n.149+3933_149+3934delinsGA