Canonical Allele Identifier: CA3261178833
Community Standard Title: NM_058216.3(RAD51C):c.589_591delinsTGA (p.Glu197Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703213_58703215delinsTGA , CM000679.2:g.58703213_58703215delinsTGA GRCh38
NC_000017.10:g.56780574_56780576delinsTGA , CM000679.1:g.56780574_56780576delinsTGA GRCh37
NC_000017.9:g.54135573_54135575delinsTGA NCBI36
NG_023199.1:g.15612_15614delinsTGA , LRG_314:g.15612_15614delinsTGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.589_591delinsTGA MANE Select NP_478123.1:p.Glu197Ter
ENST00000337432.9:c.589_591delinsTGA MANE Select ENSP00000336701.4:p.Glu197Ter
NM_058216.2:c.589_591delinsTGA NP_478123.1:p.Glu197Ter
NR_103872.1:n.493_495delinsTGA
NR_103872.2:n.464_466delinsTGA
ENST00000337432.8:c.589_591delinsTGA ENSP00000336701.4:p.Glu197Ter
ENST00000413590.5:c.227_229delinsTGA
ENST00000425173.5:c.385_387delinsTGA ENSP00000407282.1:p.Glu129Ter
ENST00000461271.5:c.238_240delinsTGA ENSP00000464056.1:p.Glu80Ter
ENST00000461271.6:c.238_240delinsTGA ENSP00000464056.2:p.Glu80Ter
ENST00000475762.5:c.*1292_*1294delinsTGA ENSP00000432421.1:n.*1292_*1294delinsTGA
ENST00000482007.5:c.*17_*19delinsTGA ENSP00000433332.1:n.*17_*19delinsTGA
ENST00000487525.5:c.*17_*19delinsTGA ENSP00000431637.1:n.*17_*19delinsTGA
ENST00000487921.5:n.501_503delinsTGA
ENST00000583539.5:c.589_591delinsTGA ENSP00000463121.1:p.Glu197Ter
ENST00000584617.5:c.311_313delinsTGA
ENST00000697677.1:n.1670_1672delinsTGA
ENST00000697678.1:n.491_493delinsTGA
ENST00000697679.1:n.1663_1665delinsTGA
ENST00000697680.1:c.*1453_*1455delinsTGA ENSP00000513392.1:n.*1453_*1455delinsTGA
ENST00000697681.1:c.*1605_*1607delinsTGA ENSP00000513393.1:n.*1605_*1607delinsTGA
ENST00000697683.1:c.*1453_*1455delinsTGA ENSP00000513395.1:n.*1453_*1455delinsTGA
ENST00000697684.1:n.649_651delinsTGA
ENST00000697685.1:c.*1286_*1288delinsTGA ENSP00000513396.1:n.*1286_*1288delinsTGA
ENST00000697686.1:c.238_240delinsTGA ENSP00000513397.1:p.Glu80Ter
ENST00000697687.1:n.468_470delinsTGA
ENST00000697688.1:n.635_637delinsTGA
ENST00000697689.1:c.*1125_*1127delinsTGA ENSP00000513398.1:n.*1125_*1127delinsTGA
ENST00000697690.1:c.589_591delinsTGA ENSP00000513399.1:p.Glu197Ter
ENST00000697691.1:c.*561_*563delinsTGA ENSP00000513400.1:n.*561_*563delinsTGA
ENST00000697692.1:c.*601_*603delinsTGA ENSP00000513401.1:n.*601_*603delinsTGA
ENST00000697694.1:c.238_240delinsTGA ENSP00000513402.1:p.Glu80Ter
ENST00000697695.1:n.1196_1198delinsTGA
XM_006722001.2:c.589_591delinsTGA XP_006722064.1:p.Glu197Ter
XM_006722001.4:c.589_591delinsTGA XP_006722064.1:p.Glu197Ter
XM_006722002.2:c.589_591delinsTGA XP_006722065.1:p.Glu197Ter
XM_006722002.4:c.589_591delinsTGA XP_006722065.1:p.Glu197Ter
XM_006722004.2:c.238_240delinsTGA XP_006722067.1:p.Glu80Ter
XM_006722004.3:c.238_240delinsTGA XP_006722067.1:p.Glu80Ter
XM_006722005.2:c.238_240delinsTGA XP_006722068.1:p.Glu80Ter
XM_006722005.3:c.238_240delinsTGA XP_006722068.1:p.Glu80Ter
XM_011525092.1:c.238_240delinsTGA XP_011523394.1:p.Glu80Ter
XM_011525092.2:c.238_240delinsTGA XP_011523394.1:p.Glu80Ter
XM_011525093.1:c.238_240delinsTGA XP_011523395.1:p.Glu80Ter
XM_011525093.2:c.238_240delinsTGA XP_011523395.1:p.Glu80Ter
XM_011525094.1:c.238_240delinsTGA XP_011523396.1:p.Glu80Ter
XM_011525094.2:c.238_240delinsTGA XP_011523396.1:p.Glu80Ter
XM_017024914.1:c.238_240delinsTGA XP_016880403.1:p.Glu80Ter
XM_017024915.1:c.238_240delinsTGA XP_016880404.1:p.Glu80Ter
XM_017024916.1:c.238_240delinsTGA XP_016880405.1:p.Glu80Ter
XM_017024917.1:c.238_240delinsTGA XP_016880406.1:p.Glu80Ter
XM_017024918.2:c.238_240delinsTGA XP_016880407.1:p.Glu80Ter
XM_017024919.1:c.238_240delinsTGA XP_016880408.1:p.Glu80Ter
XR_934513.1:n.662_664delinsTGA
XR_934513.3:n.1093_1095delinsTGA
XR_934514.1:n.662_664delinsTGA
XR_934514.3:n.1093_1095delinsTGA