Canonical Allele Identifier: CA3261179095
Community Standard Title: NM_058216.3(RAD51C):c.734_735delinsTG (p.Ala245Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709887_58709888delinsTG , CM000679.2:g.58709887_58709888delinsTG GRCh38
NC_000017.10:g.56787248_56787249delinsTG , CM000679.1:g.56787248_56787249delinsTG GRCh37
NC_000017.9:g.54142247_54142248delinsTG NCBI36
NG_023199.1:g.22286_22287delinsTG , LRG_314:g.22286_22287delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.734_735delinsTG MANE Select NP_478123.1:p.Ala245Val
ENST00000337432.9:c.734_735delinsTG MANE Select ENSP00000336701.4:p.Ala245Val
NM_058216.2:c.734_735delinsTG NP_478123.1:p.Ala245Val
NR_103872.1:n.638_639delinsTG
NR_103872.2:n.609_610delinsTG
ENST00000337432.8:c.734_735delinsTG ENSP00000336701.4:p.Ala245Val
ENST00000413590.5:c.372_373delinsTG
ENST00000461271.5:c.383_384delinsTG ENSP00000464056.1:p.Ala128Val
ENST00000461271.6:c.383_384delinsTG ENSP00000464056.2:p.Ala128Val
ENST00000475762.5:c.*1437_*1438delinsTG ENSP00000432421.1:n.*1437_*1438delinsTG
ENST00000482007.5:c.*162_*163delinsTG ENSP00000433332.1:n.*162_*163delinsTG
ENST00000487525.5:c.*307_*308delinsTG ENSP00000431637.1:n.*307_*308delinsTG
ENST00000578151.1:n.69_70delinsTG
ENST00000581221.5:n.249_250delinsTG
ENST00000583539.5:c.734_735delinsTG ENSP00000463121.1:p.Ala245Val
ENST00000584617.5:c.456_457delinsTG
ENST00000584804.1:c.29_30delinsTG ENSP00000463658.1:p.Ala10Val
ENST00000697678.1:n.636_637delinsTG
ENST00000697679.1:n.1808_1809delinsTG
ENST00000697680.1:c.*1598_*1599delinsTG ENSP00000513392.1:n.*1598_*1599delinsTG
ENST00000697681.1:c.*1895_*1896delinsTG ENSP00000513393.1:n.*1895_*1896delinsTG
ENST00000697683.1:c.*1598_*1599delinsTG ENSP00000513395.1:n.*1598_*1599delinsTG
ENST00000697684.1:n.794_795delinsTG
ENST00000697685.1:c.*1431_*1432delinsTG ENSP00000513396.1:n.*1431_*1432delinsTG
ENST00000697686.1:c.383_384delinsTG ENSP00000513397.1:p.Ala128Val
ENST00000697687.1:n.613_614delinsTG
ENST00000697688.1:n.780_781delinsTG
ENST00000697689.1:c.*1270_*1271delinsTG ENSP00000513398.1:n.*1270_*1271delinsTG
ENST00000697690.1:c.734_735delinsTG ENSP00000513399.1:p.Ala245Val
ENST00000697691.1:c.*706_*707delinsTG ENSP00000513400.1:n.*706_*707delinsTG
ENST00000697692.1:c.*746_*747delinsTG ENSP00000513401.1:n.*746_*747delinsTG
ENST00000697694.1:c.383_384delinsTG ENSP00000513402.1:p.Ala128Val
ENST00000697695.1:n.1341_1342delinsTG
XM_006722001.2:c.734_735delinsTG XP_006722064.1:p.Ala245Val
XM_006722001.4:c.734_735delinsTG XP_006722064.1:p.Ala245Val
XM_006722002.2:c.734_735delinsTG XP_006722065.1:p.Ala245Val
XM_006722002.4:c.734_735delinsTG XP_006722065.1:p.Ala245Val
XM_006722004.2:c.383_384delinsTG XP_006722067.1:p.Ala128Val
XM_006722004.3:c.383_384delinsTG XP_006722067.1:p.Ala128Val
XM_006722005.2:c.383_384delinsTG XP_006722068.1:p.Ala128Val
XM_006722005.3:c.383_384delinsTG XP_006722068.1:p.Ala128Val
XM_011525092.1:c.383_384delinsTG XP_011523394.1:p.Ala128Val
XM_011525092.2:c.383_384delinsTG XP_011523394.1:p.Ala128Val
XM_011525093.1:c.383_384delinsTG XP_011523395.1:p.Ala128Val
XM_011525093.2:c.383_384delinsTG XP_011523395.1:p.Ala128Val
XM_011525094.1:c.383_384delinsTG XP_011523396.1:p.Ala128Val
XM_011525094.2:c.383_384delinsTG XP_011523396.1:p.Ala128Val
XM_017024914.1:c.383_384delinsTG XP_016880403.1:p.Ala128Val
XM_017024915.1:c.383_384delinsTG XP_016880404.1:p.Ala128Val
XM_017024916.1:c.383_384delinsTG XP_016880405.1:p.Ala128Val
XM_017024917.1:c.383_384delinsTG XP_016880406.1:p.Ala128Val
XM_017024918.2:c.383_384delinsTG XP_016880407.1:p.Ala128Val
XM_017024919.1:c.383_384delinsTG XP_016880408.1:p.Ala128Val
XR_934513.1:n.952_953delinsTG
XR_934513.3:n.1383_1384delinsTG
XR_934514.1:n.952_953delinsTG
XR_934514.3:n.1383_1384delinsTG