Canonical Allele Identifier: CA3057243413
Community Standard Title: NM_058216.3(RAD51C):c.1036_1037delinsCC (p.Phe346Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734127_58734128delinsCC , CM000679.2:g.58734127_58734128delinsCC GRCh38
NC_000017.10:g.56811488_56811489delinsCC , CM000679.1:g.56811488_56811489delinsCC GRCh37
NC_000017.9:g.54166487_54166488delinsCC NCBI36
NG_023199.1:g.46526_46527delinsCC , LRG_314:g.46526_46527delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1036_1037delinsCC MANE Select NP_478123.1:p.Phe346Pro
ENST00000337432.9:c.1036_1037delinsCC MANE Select ENSP00000336701.4:p.Phe346Pro
NM_058216.2:c.1036_1037delinsCC NP_478123.1:p.Phe346Pro
NR_103872.1:n.940_941delinsCC
NR_103872.2:n.911_912delinsCC
ENST00000337432.8:c.1036_1037delinsCC ENSP00000336701.4:p.Phe346Pro
ENST00000413590.5:c.677_678delinsCC
ENST00000461271.6:c.*1568_*1569delinsCC ENSP00000464056.2:n.*1568_*1569delinsCC
ENST00000461706.1:n.223_224delinsCC
ENST00000475762.5:c.*1672_*1673delinsCC ENSP00000432421.1:n.*1672_*1673delinsCC
ENST00000482007.5:c.*464_*465delinsCC ENSP00000433332.1:n.*464_*465delinsCC
ENST00000487525.5:c.*612_*613delinsCC ENSP00000431637.1:n.*612_*613delinsCC
ENST00000578151.1:n.249_250delinsCC
ENST00000581221.5:n.551_552delinsCC
ENST00000584804.1:c.270_271delinsCC ENSP00000463658.1:p.Asp90=
ENST00000697680.1:c.*2000_*2001delinsCC ENSP00000513392.1:n.*2000_*2001delinsCC
ENST00000697681.1:c.*2197_*2198delinsCC ENSP00000513393.1:n.*2197_*2198delinsCC
ENST00000697683.1:c.*1972_*1973delinsCC ENSP00000513395.1:n.*1972_*1973delinsCC
ENST00000697685.1:c.*1733_*1734delinsCC ENSP00000513396.1:n.*1733_*1734delinsCC
ENST00000697686.1:c.807_808delinsCC ENSP00000513397.1:p.Asp269=
ENST00000697689.1:c.*1450_*1451delinsCC ENSP00000513398.1:n.*1450_*1451delinsCC
ENST00000697690.1:c.914_915delinsCC ENSP00000513399.1:p.Ile305Thr
ENST00000697691.1:c.*1008_*1009delinsCC ENSP00000513400.1:n.*1008_*1009delinsCC
ENST00000697692.1:c.*1048_*1049delinsCC ENSP00000513401.1:n.*1048_*1049delinsCC
ENST00000697694.1:c.685_686delinsCC ENSP00000513402.1:p.Phe229Pro
ENST00000697695.1:n.1643_1644delinsCC
XM_006722001.2:c.1039_1040delinsCC XP_006722064.1:p.Phe347Pro
XM_006722001.4:c.1039_1040delinsCC XP_006722064.1:p.Phe347Pro
XM_006722002.2:c.975_976delinsCC XP_006722065.1:p.Asp325=
XM_006722002.4:c.975_976delinsCC XP_006722065.1:p.Asp325=
XM_006722004.2:c.688_689delinsCC XP_006722067.1:p.Phe230Pro
XM_006722004.3:c.688_689delinsCC XP_006722067.1:p.Phe230Pro
XM_006722005.2:c.688_689delinsCC XP_006722068.1:p.Phe230Pro
XM_006722005.3:c.688_689delinsCC XP_006722068.1:p.Phe230Pro
XM_011525092.1:c.688_689delinsCC XP_011523394.1:p.Phe230Pro
XM_011525092.2:c.688_689delinsCC XP_011523394.1:p.Phe230Pro
XM_011525093.1:c.688_689delinsCC XP_011523395.1:p.Phe230Pro
XM_011525093.2:c.688_689delinsCC XP_011523395.1:p.Phe230Pro
XM_011525094.1:c.688_689delinsCC XP_011523396.1:p.Phe230Pro
XM_011525094.2:c.688_689delinsCC XP_011523396.1:p.Phe230Pro
XM_017024914.1:c.685_686delinsCC XP_016880403.1:p.Phe229Pro
XM_017024915.1:c.685_686delinsCC XP_016880404.1:p.Phe229Pro
XM_017024916.1:c.685_686delinsCC XP_016880405.1:p.Phe229Pro
XM_017024917.1:c.685_686delinsCC XP_016880406.1:p.Phe229Pro
XM_017024918.2:c.685_686delinsCC XP_016880407.1:p.Phe229Pro
XM_017024919.1:c.624_625delinsCC XP_016880408.1:p.Asp208=
XR_934513.1:n.1254_1255delinsCC
XR_934513.3:n.1685_1686delinsCC
XR_934514.1:n.1257_1258delinsCC
XR_934514.3:n.1688_1689delinsCC
XR_934886.1:n.149+3943_149+3944delinsGG
XR_934886.2:n.149+3943_149+3944delinsGG