Canonical Allele Identifier: CA3060598411
Community Standard Title: NM_058216.3(RAD51C):c.722_723delinsCC (p.Val241Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709875_58709876delinsCC , CM000679.2:g.58709875_58709876delinsCC GRCh38
NC_000017.10:g.56787236_56787237delinsCC , CM000679.1:g.56787236_56787237delinsCC GRCh37
NC_000017.9:g.54142235_54142236delinsCC NCBI36
NG_023199.1:g.22274_22275delinsCC , LRG_314:g.22274_22275delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.722_723delinsCC MANE Select NP_478123.1:p.Val241Ala
ENST00000337432.9:c.722_723delinsCC MANE Select ENSP00000336701.4:p.Val241Ala
NM_058216.2:c.722_723delinsCC NP_478123.1:p.Val241Ala
NR_103872.1:n.626_627delinsCC
NR_103872.2:n.597_598delinsCC
ENST00000337432.8:c.722_723delinsCC ENSP00000336701.4:p.Val241Ala
ENST00000413590.5:c.360_361delinsCC
ENST00000425173.5:c.638_639delinsCC ENSP00000407282.1:p.Val213Ala
ENST00000461271.5:c.371_372delinsCC ENSP00000464056.1:p.Val124Ala
ENST00000461271.6:c.371_372delinsCC ENSP00000464056.2:p.Val124Ala
ENST00000475762.5:c.*1425_*1426delinsCC ENSP00000432421.1:n.*1425_*1426delinsCC
ENST00000482007.5:c.*150_*151delinsCC ENSP00000433332.1:n.*150_*151delinsCC
ENST00000487525.5:c.*295_*296delinsCC ENSP00000431637.1:n.*295_*296delinsCC
ENST00000578151.1:n.57_58delinsCC
ENST00000581221.5:n.237_238delinsCC
ENST00000583539.5:c.722_723delinsCC ENSP00000463121.1:p.Val241Ala
ENST00000584617.5:c.444_445delinsCC
ENST00000584804.1:c.17_18delinsCC ENSP00000463658.1:p.Val6Ala
ENST00000697678.1:n.624_625delinsCC
ENST00000697679.1:n.1796_1797delinsCC
ENST00000697680.1:c.*1586_*1587delinsCC ENSP00000513392.1:n.*1586_*1587delinsCC
ENST00000697681.1:c.*1883_*1884delinsCC ENSP00000513393.1:n.*1883_*1884delinsCC
ENST00000697683.1:c.*1586_*1587delinsCC ENSP00000513395.1:n.*1586_*1587delinsCC
ENST00000697684.1:n.782_783delinsCC
ENST00000697685.1:c.*1419_*1420delinsCC ENSP00000513396.1:n.*1419_*1420delinsCC
ENST00000697686.1:c.371_372delinsCC ENSP00000513397.1:p.Val124Ala
ENST00000697687.1:n.601_602delinsCC
ENST00000697688.1:n.768_769delinsCC
ENST00000697689.1:c.*1258_*1259delinsCC ENSP00000513398.1:n.*1258_*1259delinsCC
ENST00000697690.1:c.722_723delinsCC ENSP00000513399.1:p.Val241Ala
ENST00000697691.1:c.*694_*695delinsCC ENSP00000513400.1:n.*694_*695delinsCC
ENST00000697692.1:c.*734_*735delinsCC ENSP00000513401.1:n.*734_*735delinsCC
ENST00000697694.1:c.371_372delinsCC ENSP00000513402.1:p.Val124Ala
ENST00000697695.1:n.1329_1330delinsCC
XM_006722001.2:c.722_723delinsCC XP_006722064.1:p.Val241Ala
XM_006722001.4:c.722_723delinsCC XP_006722064.1:p.Val241Ala
XM_006722002.2:c.722_723delinsCC XP_006722065.1:p.Val241Ala
XM_006722002.4:c.722_723delinsCC XP_006722065.1:p.Val241Ala
XM_006722004.2:c.371_372delinsCC XP_006722067.1:p.Val124Ala
XM_006722004.3:c.371_372delinsCC XP_006722067.1:p.Val124Ala
XM_006722005.2:c.371_372delinsCC XP_006722068.1:p.Val124Ala
XM_006722005.3:c.371_372delinsCC XP_006722068.1:p.Val124Ala
XM_011525092.1:c.371_372delinsCC XP_011523394.1:p.Val124Ala
XM_011525092.2:c.371_372delinsCC XP_011523394.1:p.Val124Ala
XM_011525093.1:c.371_372delinsCC XP_011523395.1:p.Val124Ala
XM_011525093.2:c.371_372delinsCC XP_011523395.1:p.Val124Ala
XM_011525094.1:c.371_372delinsCC XP_011523396.1:p.Val124Ala
XM_011525094.2:c.371_372delinsCC XP_011523396.1:p.Val124Ala
XM_017024914.1:c.371_372delinsCC XP_016880403.1:p.Val124Ala
XM_017024915.1:c.371_372delinsCC XP_016880404.1:p.Val124Ala
XM_017024916.1:c.371_372delinsCC XP_016880405.1:p.Val124Ala
XM_017024917.1:c.371_372delinsCC XP_016880406.1:p.Val124Ala
XM_017024918.2:c.371_372delinsCC XP_016880407.1:p.Val124Ala
XM_017024919.1:c.371_372delinsCC XP_016880408.1:p.Val124Ala
XR_934513.1:n.940_941delinsCC
XR_934513.3:n.1371_1372delinsCC
XR_934514.1:n.940_941delinsCC
XR_934514.3:n.1371_1372delinsCC