Canonical Allele Identifier: CA3261180858
Community Standard Title: NM_058216.3(RAD51C):c.1123_1125delinsAAG (p.Glu375Lys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734214_58734216delinsAAG , CM000679.2:g.58734214_58734216delinsAAG GRCh38
NC_000017.10:g.56811575_56811577delinsAAG , CM000679.1:g.56811575_56811577delinsAAG GRCh37
NC_000017.9:g.54166574_54166576delinsAAG NCBI36
NG_023199.1:g.46613_46615delinsAAG , LRG_314:g.46613_46615delinsAAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1123_1125delinsAAG MANE Select NP_478123.1:p.Glu375Lys
ENST00000337432.9:c.1123_1125delinsAAG MANE Select ENSP00000336701.4:p.Glu375Lys
NM_058216.2:c.1123_1125delinsAAG NP_478123.1:p.Glu375Lys
NR_103872.1:n.1027_1029delinsAAG
NR_103872.2:n.998_1000delinsAAG
ENST00000337432.8:c.1123_1125delinsAAG ENSP00000336701.4:p.Glu375Lys
ENST00000413590.5:c.764_766delinsAAG
ENST00000461271.6:c.*1655_*1657delinsAAG ENSP00000464056.2:n.*1655_*1657delinsAAG
ENST00000461706.1:n.310_312delinsAAG
ENST00000475762.5:c.*1759_*1761delinsAAG ENSP00000432421.1:n.*1759_*1761delinsAAG
ENST00000482007.5:c.*551_*553delinsAAG ENSP00000433332.1:n.*551_*553delinsAAG
ENST00000487525.5:c.*699_*701delinsAAG ENSP00000431637.1:n.*699_*701delinsAAG
ENST00000578151.1:n.336_338delinsAAG
ENST00000581221.5:n.638_640delinsAAG
ENST00000584804.1:c.357_359delinsAAG ENSP00000463658.1:n.357_359delinsAAG
ENST00000697680.1:c.*2087_*2089delinsAAG ENSP00000513392.1:n.*2087_*2089delinsAAG
ENST00000697681.1:c.*2284_*2286delinsAAG ENSP00000513393.1:n.*2284_*2286delinsAAG
ENST00000697683.1:c.*2059_*2061delinsAAG ENSP00000513395.1:n.*2059_*2061delinsAAG
ENST00000697685.1:c.*1820_*1822delinsAAG ENSP00000513396.1:n.*1820_*1822delinsAAG
ENST00000697686.1:c.*33_*35delinsAAG ENSP00000513397.1:n.*33_*35delinsAAG
ENST00000697689.1:c.*1537_*1539delinsAAG ENSP00000513398.1:n.*1537_*1539delinsAAG
ENST00000697690.1:c.*83_*85delinsAAG ENSP00000513399.1:n.*83_*85delinsAAG
ENST00000697691.1:c.*1095_*1097delinsAAG ENSP00000513400.1:n.*1095_*1097delinsAAG
ENST00000697692.1:c.*1135_*1137delinsAAG ENSP00000513401.1:n.*1135_*1137delinsAAG
ENST00000697694.1:c.772_774delinsAAG ENSP00000513402.1:p.Glu258Lys
ENST00000697695.1:n.1730_1732delinsAAG
XM_006722001.2:c.1126_1128delinsAAG XP_006722064.1:p.Glu376Lys
XM_006722001.4:c.1126_1128delinsAAG XP_006722064.1:p.Glu376Lys
XM_006722002.2:c.*33_*35delinsAAG XP_006722065.1:n.*33_*35delinsAAG
XM_006722002.4:c.*33_*35delinsAAG XP_006722065.1:n.*33_*35delinsAAG
XM_006722004.2:c.775_777delinsAAG XP_006722067.1:p.Glu259Lys
XM_006722004.3:c.775_777delinsAAG XP_006722067.1:p.Glu259Lys
XM_006722005.2:c.775_777delinsAAG XP_006722068.1:p.Glu259Lys
XM_006722005.3:c.775_777delinsAAG XP_006722068.1:p.Glu259Lys
XM_011525092.1:c.775_777delinsAAG XP_011523394.1:p.Glu259Lys
XM_011525092.2:c.775_777delinsAAG XP_011523394.1:p.Glu259Lys
XM_011525093.1:c.775_777delinsAAG XP_011523395.1:p.Glu259Lys
XM_011525093.2:c.775_777delinsAAG XP_011523395.1:p.Glu259Lys
XM_011525094.1:c.775_777delinsAAG XP_011523396.1:p.Glu259Lys
XM_011525094.2:c.775_777delinsAAG XP_011523396.1:p.Glu259Lys
XM_017024914.1:c.772_774delinsAAG XP_016880403.1:p.Glu258Lys
XM_017024915.1:c.772_774delinsAAG XP_016880404.1:p.Glu258Lys
XM_017024916.1:c.772_774delinsAAG XP_016880405.1:p.Glu258Lys
XM_017024917.1:c.772_774delinsAAG XP_016880406.1:p.Glu258Lys
XM_017024918.2:c.772_774delinsAAG XP_016880407.1:p.Glu258Lys
XM_017024919.1:c.*33_*35delinsAAG XP_016880408.1:n.*33_*35delinsAAG
XR_934513.1:n.1341_1343delinsAAG
XR_934513.3:n.1772_1774delinsAAG
XR_934886.1:n.149+3855_149+3857delinsCTT
XR_934886.2:n.149+3855_149+3857delinsCTT