Canonical Allele Identifier: CA3261180264
Community Standard Title: NM_058216.3(RAD51C):c.811_813delinsGGA (p.Ser271Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709964_58709966delinsGGA , CM000679.2:g.58709964_58709966delinsGGA GRCh38
NC_000017.10:g.56787325_56787327delinsGGA , CM000679.1:g.56787325_56787327delinsGGA GRCh37
NC_000017.9:g.54142324_54142326delinsGGA NCBI36
NG_023199.1:g.22363_22365delinsGGA , LRG_314:g.22363_22365delinsGGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.811_813delinsGGA MANE Select NP_478123.1:p.Ser271Gly
ENST00000337432.9:c.811_813delinsGGA MANE Select ENSP00000336701.4:p.Ser271Gly
NM_058216.2:c.811_813delinsGGA NP_478123.1:p.Ser271Gly
NR_103872.1:n.715_717delinsGGA
NR_103872.2:n.686_688delinsGGA
ENST00000337432.8:c.811_813delinsGGA ENSP00000336701.4:p.Ser271Gly
ENST00000413590.5:c.449_451delinsGGA
ENST00000461271.6:c.460_462delinsGGA ENSP00000464056.2:p.Ser154Gly
ENST00000475762.5:c.*1514_*1516delinsGGA ENSP00000432421.1:n.*1514_*1516delinsGGA
ENST00000482007.5:c.*239_*241delinsGGA ENSP00000433332.1:n.*239_*241delinsGGA
ENST00000487525.5:c.*384_*386delinsGGA ENSP00000431637.1:n.*384_*386delinsGGA
ENST00000578151.1:n.146_148delinsGGA
ENST00000581221.5:n.326_328delinsGGA
ENST00000583539.5:c.811_813delinsGGA ENSP00000463121.1:p.Ser271Gly
ENST00000584617.5:c.533_535delinsGGA
ENST00000584804.1:c.106_108delinsGGA ENSP00000463658.1:p.Ser36Gly
ENST00000697678.1:n.713_715delinsGGA
ENST00000697679.1:n.1885_1887delinsGGA
ENST00000697680.1:c.*1675_*1677delinsGGA ENSP00000513392.1:n.*1675_*1677delinsGGA
ENST00000697681.1:c.*1972_*1974delinsGGA ENSP00000513393.1:n.*1972_*1974delinsGGA
ENST00000697683.1:c.*1675_*1677delinsGGA ENSP00000513395.1:n.*1675_*1677delinsGGA
ENST00000697684.1:n.871_873delinsGGA
ENST00000697685.1:c.*1508_*1510delinsGGA ENSP00000513396.1:n.*1508_*1510delinsGGA
ENST00000697686.1:c.460_462delinsGGA ENSP00000513397.1:p.Ser154Gly
ENST00000697687.1:n.690_692delinsGGA
ENST00000697688.1:n.857_859delinsGGA
ENST00000697689.1:c.*1347_*1349delinsGGA ENSP00000513398.1:n.*1347_*1349delinsGGA
ENST00000697690.1:c.811_813delinsGGA ENSP00000513399.1:p.Ser271Gly
ENST00000697691.1:c.*783_*785delinsGGA ENSP00000513400.1:n.*783_*785delinsGGA
ENST00000697692.1:c.*823_*825delinsGGA ENSP00000513401.1:n.*823_*825delinsGGA
ENST00000697694.1:c.460_462delinsGGA ENSP00000513402.1:p.Ser154Gly
ENST00000697695.1:n.1418_1420delinsGGA
XM_006722001.2:c.811_813delinsGGA XP_006722064.1:p.Ser271Gly
XM_006722001.4:c.811_813delinsGGA XP_006722064.1:p.Ser271Gly
XM_006722002.2:c.811_813delinsGGA XP_006722065.1:p.Ser271Gly
XM_006722002.4:c.811_813delinsGGA XP_006722065.1:p.Ser271Gly
XM_006722004.2:c.460_462delinsGGA XP_006722067.1:p.Ser154Gly
XM_006722004.3:c.460_462delinsGGA XP_006722067.1:p.Ser154Gly
XM_006722005.2:c.460_462delinsGGA XP_006722068.1:p.Ser154Gly
XM_006722005.3:c.460_462delinsGGA XP_006722068.1:p.Ser154Gly
XM_011525092.1:c.460_462delinsGGA XP_011523394.1:p.Ser154Gly
XM_011525092.2:c.460_462delinsGGA XP_011523394.1:p.Ser154Gly
XM_011525093.1:c.460_462delinsGGA XP_011523395.1:p.Ser154Gly
XM_011525093.2:c.460_462delinsGGA XP_011523395.1:p.Ser154Gly
XM_011525094.1:c.460_462delinsGGA XP_011523396.1:p.Ser154Gly
XM_011525094.2:c.460_462delinsGGA XP_011523396.1:p.Ser154Gly
XM_017024914.1:c.460_462delinsGGA XP_016880403.1:p.Ser154Gly
XM_017024915.1:c.460_462delinsGGA XP_016880404.1:p.Ser154Gly
XM_017024916.1:c.460_462delinsGGA XP_016880405.1:p.Ser154Gly
XM_017024917.1:c.460_462delinsGGA XP_016880406.1:p.Ser154Gly
XM_017024918.2:c.460_462delinsGGA XP_016880407.1:p.Ser154Gly
XM_017024919.1:c.460_462delinsGGA XP_016880408.1:p.Ser154Gly
XR_934513.1:n.1029_1031delinsGGA
XR_934513.3:n.1460_1462delinsGGA
XR_934514.1:n.1029_1031delinsGGA
XR_934514.3:n.1460_1462delinsGGA