Canonical Allele Identifier: CA3261180831
Community Standard Title: NM_058216.3(RAD51C):c.1120_1122delinsAAG (p.Glu374Lys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734211_58734213delinsAAG , CM000679.2:g.58734211_58734213delinsAAG GRCh38
NC_000017.10:g.56811572_56811574delinsAAG , CM000679.1:g.56811572_56811574delinsAAG GRCh37
NC_000017.9:g.54166571_54166573delinsAAG NCBI36
NG_023199.1:g.46610_46612delinsAAG , LRG_314:g.46610_46612delinsAAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1120_1122delinsAAG MANE Select NP_478123.1:p.Glu374Lys
ENST00000337432.9:c.1120_1122delinsAAG MANE Select ENSP00000336701.4:p.Glu374Lys
NM_058216.2:c.1120_1122delinsAAG NP_478123.1:p.Glu374Lys
NR_103872.1:n.1024_1026delinsAAG
NR_103872.2:n.995_997delinsAAG
ENST00000337432.8:c.1120_1122delinsAAG ENSP00000336701.4:p.Glu374Lys
ENST00000413590.5:c.761_763delinsAAG
ENST00000461271.6:c.*1652_*1654delinsAAG ENSP00000464056.2:n.*1652_*1654delinsAAG
ENST00000461706.1:n.307_309delinsAAG
ENST00000475762.5:c.*1756_*1758delinsAAG ENSP00000432421.1:n.*1756_*1758delinsAAG
ENST00000482007.5:c.*548_*550delinsAAG ENSP00000433332.1:n.*548_*550delinsAAG
ENST00000487525.5:c.*696_*698delinsAAG ENSP00000431637.1:n.*696_*698delinsAAG
ENST00000578151.1:n.333_335delinsAAG
ENST00000581221.5:n.635_637delinsAAG
ENST00000584804.1:c.354_356delinsAAG ENSP00000463658.1:n.354_356delinsAAG
ENST00000697680.1:c.*2084_*2086delinsAAG ENSP00000513392.1:n.*2084_*2086delinsAAG
ENST00000697681.1:c.*2281_*2283delinsAAG ENSP00000513393.1:n.*2281_*2283delinsAAG
ENST00000697683.1:c.*2056_*2058delinsAAG ENSP00000513395.1:n.*2056_*2058delinsAAG
ENST00000697685.1:c.*1817_*1819delinsAAG ENSP00000513396.1:n.*1817_*1819delinsAAG
ENST00000697686.1:c.*30_*32delinsAAG ENSP00000513397.1:n.*30_*32delinsAAG
ENST00000697689.1:c.*1534_*1536delinsAAG ENSP00000513398.1:n.*1534_*1536delinsAAG
ENST00000697690.1:c.*80_*82delinsAAG ENSP00000513399.1:n.*80_*82delinsAAG
ENST00000697691.1:c.*1092_*1094delinsAAG ENSP00000513400.1:n.*1092_*1094delinsAAG
ENST00000697692.1:c.*1132_*1134delinsAAG ENSP00000513401.1:n.*1132_*1134delinsAAG
ENST00000697694.1:c.769_771delinsAAG ENSP00000513402.1:p.Glu257Lys
ENST00000697695.1:n.1727_1729delinsAAG
XM_006722001.2:c.1123_1125delinsAAG XP_006722064.1:p.Glu375Lys
XM_006722001.4:c.1123_1125delinsAAG XP_006722064.1:p.Glu375Lys
XM_006722002.2:c.*30_*32delinsAAG XP_006722065.1:n.*30_*32delinsAAG
XM_006722002.4:c.*30_*32delinsAAG XP_006722065.1:n.*30_*32delinsAAG
XM_006722004.2:c.772_774delinsAAG XP_006722067.1:p.Glu258Lys
XM_006722004.3:c.772_774delinsAAG XP_006722067.1:p.Glu258Lys
XM_006722005.2:c.772_774delinsAAG XP_006722068.1:p.Glu258Lys
XM_006722005.3:c.772_774delinsAAG XP_006722068.1:p.Glu258Lys
XM_011525092.1:c.772_774delinsAAG XP_011523394.1:p.Glu258Lys
XM_011525092.2:c.772_774delinsAAG XP_011523394.1:p.Glu258Lys
XM_011525093.1:c.772_774delinsAAG XP_011523395.1:p.Glu258Lys
XM_011525093.2:c.772_774delinsAAG XP_011523395.1:p.Glu258Lys
XM_011525094.1:c.772_774delinsAAG XP_011523396.1:p.Glu258Lys
XM_011525094.2:c.772_774delinsAAG XP_011523396.1:p.Glu258Lys
XM_017024914.1:c.769_771delinsAAG XP_016880403.1:p.Glu257Lys
XM_017024915.1:c.769_771delinsAAG XP_016880404.1:p.Glu257Lys
XM_017024916.1:c.769_771delinsAAG XP_016880405.1:p.Glu257Lys
XM_017024917.1:c.769_771delinsAAG XP_016880406.1:p.Glu257Lys
XM_017024918.2:c.769_771delinsAAG XP_016880407.1:p.Glu257Lys
XM_017024919.1:c.*30_*32delinsAAG XP_016880408.1:n.*30_*32delinsAAG
XR_934513.1:n.1338_1340delinsAAG
XR_934513.3:n.1769_1771delinsAAG
XR_934886.1:n.149+3858_149+3860delinsCTT
XR_934886.2:n.149+3858_149+3860delinsCTT