Canonical Allele Identifier: CA3261179600
Community Standard Title: NM_058216.3(RAD51C):c.644_645delinsGA (p.Asp215Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703268_58703269delinsGA , CM000679.2:g.58703268_58703269delinsGA GRCh38
NC_000017.10:g.56780629_56780630delinsGA , CM000679.1:g.56780629_56780630delinsGA GRCh37
NC_000017.9:g.54135628_54135629delinsGA NCBI36
NG_023199.1:g.15667_15668delinsGA , LRG_314:g.15667_15668delinsGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.644_645delinsGA MANE Select NP_478123.1:p.Asp215Gly
ENST00000337432.9:c.644_645delinsGA MANE Select ENSP00000336701.4:p.Asp215Gly
NM_058216.2:c.644_645delinsGA NP_478123.1:p.Asp215Gly
NR_103872.1:n.548_549delinsGA
NR_103872.2:n.519_520delinsGA
ENST00000337432.8:c.644_645delinsGA ENSP00000336701.4:p.Asp215Gly
ENST00000413590.5:c.282_283delinsGA
ENST00000425173.5:c.440_441delinsGA ENSP00000407282.1:p.Asp147Gly
ENST00000461271.5:c.293_294delinsGA ENSP00000464056.1:p.Asp98Gly
ENST00000461271.6:c.293_294delinsGA ENSP00000464056.2:p.Asp98Gly
ENST00000475762.5:c.*1347_*1348delinsGA ENSP00000432421.1:n.*1347_*1348delinsGA
ENST00000482007.5:c.*72_*73delinsGA ENSP00000433332.1:n.*72_*73delinsGA
ENST00000487525.5:c.*72_*73delinsGA ENSP00000431637.1:n.*72_*73delinsGA
ENST00000487921.5:n.556_557delinsGA
ENST00000583539.5:c.644_645delinsGA ENSP00000463121.1:p.Asp215Gly
ENST00000584617.5:c.366_367delinsGA
ENST00000697677.1:n.1725_1726delinsGA
ENST00000697678.1:n.546_547delinsGA
ENST00000697679.1:n.1718_1719delinsGA
ENST00000697680.1:c.*1508_*1509delinsGA ENSP00000513392.1:n.*1508_*1509delinsGA
ENST00000697681.1:c.*1660_*1661delinsGA ENSP00000513393.1:n.*1660_*1661delinsGA
ENST00000697683.1:c.*1508_*1509delinsGA ENSP00000513395.1:n.*1508_*1509delinsGA
ENST00000697684.1:n.704_705delinsGA
ENST00000697685.1:c.*1341_*1342delinsGA ENSP00000513396.1:n.*1341_*1342delinsGA
ENST00000697686.1:c.293_294delinsGA ENSP00000513397.1:p.Asp98Gly
ENST00000697687.1:n.523_524delinsGA
ENST00000697688.1:n.690_691delinsGA
ENST00000697689.1:c.*1180_*1181delinsGA ENSP00000513398.1:n.*1180_*1181delinsGA
ENST00000697690.1:c.644_645delinsGA ENSP00000513399.1:p.Asp215Gly
ENST00000697691.1:c.*616_*617delinsGA ENSP00000513400.1:n.*616_*617delinsGA
ENST00000697692.1:c.*656_*657delinsGA ENSP00000513401.1:n.*656_*657delinsGA
ENST00000697694.1:c.293_294delinsGA ENSP00000513402.1:p.Asp98Gly
ENST00000697695.1:n.1251_1252delinsGA
XM_006722001.2:c.644_645delinsGA XP_006722064.1:p.Asp215Gly
XM_006722001.4:c.644_645delinsGA XP_006722064.1:p.Asp215Gly
XM_006722002.2:c.644_645delinsGA XP_006722065.1:p.Asp215Gly
XM_006722002.4:c.644_645delinsGA XP_006722065.1:p.Asp215Gly
XM_006722004.2:c.293_294delinsGA XP_006722067.1:p.Asp98Gly
XM_006722004.3:c.293_294delinsGA XP_006722067.1:p.Asp98Gly
XM_006722005.2:c.293_294delinsGA XP_006722068.1:p.Asp98Gly
XM_006722005.3:c.293_294delinsGA XP_006722068.1:p.Asp98Gly
XM_011525092.1:c.293_294delinsGA XP_011523394.1:p.Asp98Gly
XM_011525092.2:c.293_294delinsGA XP_011523394.1:p.Asp98Gly
XM_011525093.1:c.293_294delinsGA XP_011523395.1:p.Asp98Gly
XM_011525093.2:c.293_294delinsGA XP_011523395.1:p.Asp98Gly
XM_011525094.1:c.293_294delinsGA XP_011523396.1:p.Asp98Gly
XM_011525094.2:c.293_294delinsGA XP_011523396.1:p.Asp98Gly
XM_017024914.1:c.293_294delinsGA XP_016880403.1:p.Asp98Gly
XM_017024915.1:c.293_294delinsGA XP_016880404.1:p.Asp98Gly
XM_017024916.1:c.293_294delinsGA XP_016880405.1:p.Asp98Gly
XM_017024917.1:c.293_294delinsGA XP_016880406.1:p.Asp98Gly
XM_017024918.2:c.293_294delinsGA XP_016880407.1:p.Asp98Gly
XM_017024919.1:c.293_294delinsGA XP_016880408.1:p.Asp98Gly
XR_934513.1:n.717_718delinsGA
XR_934513.3:n.1148_1149delinsGA
XR_934514.1:n.717_718delinsGA
XR_934514.3:n.1148_1149delinsGA