Canonical Allele Identifier: CA3057243512
Community Standard Title: NM_058216.3(RAD51C):c.1050_1051delinsCC (p.Val351Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734141_58734142delinsCC , CM000679.2:g.58734141_58734142delinsCC GRCh38
NC_000017.10:g.56811502_56811503delinsCC , CM000679.1:g.56811502_56811503delinsCC GRCh37
NC_000017.9:g.54166501_54166502delinsCC NCBI36
NG_023199.1:g.46540_46541delinsCC , LRG_314:g.46540_46541delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1050_1051delinsCC MANE Select NP_478123.1:p.Val351Leu
ENST00000337432.9:c.1050_1051delinsCC MANE Select ENSP00000336701.4:p.Val351Leu
NM_058216.2:c.1050_1051delinsCC NP_478123.1:p.Val351Leu
NR_103872.1:n.954_955delinsCC
NR_103872.2:n.925_926delinsCC
ENST00000337432.8:c.1050_1051delinsCC ENSP00000336701.4:p.Val351Leu
ENST00000413590.5:c.691_692delinsCC
ENST00000461271.6:c.*1582_*1583delinsCC ENSP00000464056.2:n.*1582_*1583delinsCC
ENST00000461706.1:n.237_238delinsCC
ENST00000475762.5:c.*1686_*1687delinsCC ENSP00000432421.1:n.*1686_*1687delinsCC
ENST00000482007.5:c.*478_*479delinsCC ENSP00000433332.1:n.*478_*479delinsCC
ENST00000487525.5:c.*626_*627delinsCC ENSP00000431637.1:n.*626_*627delinsCC
ENST00000578151.1:n.263_264delinsCC
ENST00000581221.5:n.565_566delinsCC
ENST00000584804.1:c.284_285delinsCC ENSP00000463658.1:p.Leu95Ser
ENST00000697680.1:c.*2014_*2015delinsCC ENSP00000513392.1:n.*2014_*2015delinsCC
ENST00000697681.1:c.*2211_*2212delinsCC ENSP00000513393.1:n.*2211_*2212delinsCC
ENST00000697683.1:c.*1986_*1987delinsCC ENSP00000513395.1:n.*1986_*1987delinsCC
ENST00000697685.1:c.*1747_*1748delinsCC ENSP00000513396.1:n.*1747_*1748delinsCC
ENST00000697686.1:c.821_822delinsCC ENSP00000513397.1:p.Leu274Ser
ENST00000697689.1:c.*1464_*1465delinsCC ENSP00000513398.1:n.*1464_*1465delinsCC
ENST00000697690.1:c.*10_*11delinsCC ENSP00000513399.1:n.*10_*11delinsCC
ENST00000697691.1:c.*1022_*1023delinsCC ENSP00000513400.1:n.*1022_*1023delinsCC
ENST00000697692.1:c.*1062_*1063delinsCC ENSP00000513401.1:n.*1062_*1063delinsCC
ENST00000697694.1:c.699_700delinsCC ENSP00000513402.1:p.Val234Leu
ENST00000697695.1:n.1657_1658delinsCC
XM_006722001.2:c.1053_1054delinsCC XP_006722064.1:p.Val352Leu
XM_006722001.4:c.1053_1054delinsCC XP_006722064.1:p.Val352Leu
XM_006722002.2:c.989_990delinsCC XP_006722065.1:p.Leu330Ser
XM_006722002.4:c.989_990delinsCC XP_006722065.1:p.Leu330Ser
XM_006722004.2:c.702_703delinsCC XP_006722067.1:p.Val235Leu
XM_006722004.3:c.702_703delinsCC XP_006722067.1:p.Val235Leu
XM_006722005.2:c.702_703delinsCC XP_006722068.1:p.Val235Leu
XM_006722005.3:c.702_703delinsCC XP_006722068.1:p.Val235Leu
XM_011525092.1:c.702_703delinsCC XP_011523394.1:p.Val235Leu
XM_011525092.2:c.702_703delinsCC XP_011523394.1:p.Val235Leu
XM_011525093.1:c.702_703delinsCC XP_011523395.1:p.Val235Leu
XM_011525093.2:c.702_703delinsCC XP_011523395.1:p.Val235Leu
XM_011525094.1:c.702_703delinsCC XP_011523396.1:p.Val235Leu
XM_011525094.2:c.702_703delinsCC XP_011523396.1:p.Val235Leu
XM_017024914.1:c.699_700delinsCC XP_016880403.1:p.Val234Leu
XM_017024915.1:c.699_700delinsCC XP_016880404.1:p.Val234Leu
XM_017024916.1:c.699_700delinsCC XP_016880405.1:p.Val234Leu
XM_017024917.1:c.699_700delinsCC XP_016880406.1:p.Val234Leu
XM_017024918.2:c.699_700delinsCC XP_016880407.1:p.Val234Leu
XM_017024919.1:c.638_639delinsCC XP_016880408.1:p.Leu213Ser
XR_934513.1:n.1268_1269delinsCC
XR_934513.3:n.1699_1700delinsCC
XR_934514.1:n.1271_1272delinsCC
XR_934514.3:n.1702_1703delinsCC
XR_934886.1:n.149+3929_149+3930delinsGG
XR_934886.2:n.149+3929_149+3930delinsGG