Canonical Allele Identifier: CA3060598427
Community Standard Title: NM_058216.3(RAD51C):c.1031_1032delinsCC (p.Gln344Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734122_58734123delinsCC , CM000679.2:g.58734122_58734123delinsCC GRCh38
NC_000017.10:g.56811483_56811484delinsCC , CM000679.1:g.56811483_56811484delinsCC GRCh37
NC_000017.9:g.54166482_54166483delinsCC NCBI36
NG_023199.1:g.46521_46522delinsCC , LRG_314:g.46521_46522delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1031_1032delinsCC MANE Select NP_478123.1:p.Gln344Pro
ENST00000337432.9:c.1031_1032delinsCC MANE Select ENSP00000336701.4:p.Gln344Pro
NM_058216.2:c.1031_1032delinsCC NP_478123.1:p.Gln344Pro
NR_103872.1:n.935_936delinsCC
NR_103872.2:n.906_907delinsCC
ENST00000337432.8:c.1031_1032delinsCC ENSP00000336701.4:p.Gln344Pro
ENST00000413590.5:c.672_673delinsCC
ENST00000461271.6:c.*1563_*1564delinsCC ENSP00000464056.2:n.*1563_*1564delinsCC
ENST00000461706.1:n.218_219delinsCC
ENST00000475762.5:c.*1667_*1668delinsCC ENSP00000432421.1:n.*1667_*1668delinsCC
ENST00000482007.5:c.*459_*460delinsCC ENSP00000433332.1:n.*459_*460delinsCC
ENST00000487525.5:c.*607_*608delinsCC ENSP00000431637.1:n.*607_*608delinsCC
ENST00000578151.1:n.244_245delinsCC
ENST00000581221.5:n.546_547delinsCC
ENST00000584804.1:c.265_266delinsCC ENSP00000463658.1:p.Arg89Pro
ENST00000697680.1:c.*1995_*1996delinsCC ENSP00000513392.1:n.*1995_*1996delinsCC
ENST00000697681.1:c.*2192_*2193delinsCC ENSP00000513393.1:n.*2192_*2193delinsCC
ENST00000697683.1:c.*1967_*1968delinsCC ENSP00000513395.1:n.*1967_*1968delinsCC
ENST00000697685.1:c.*1728_*1729delinsCC ENSP00000513396.1:n.*1728_*1729delinsCC
ENST00000697686.1:c.802_803delinsCC ENSP00000513397.1:p.Arg268Pro
ENST00000697689.1:c.*1445_*1446delinsCC ENSP00000513398.1:n.*1445_*1446delinsCC
ENST00000697690.1:c.909_910delinsCC ENSP00000513399.1:p.Gly304Arg
ENST00000697691.1:c.*1003_*1004delinsCC ENSP00000513400.1:n.*1003_*1004delinsCC
ENST00000697692.1:c.*1043_*1044delinsCC ENSP00000513401.1:n.*1043_*1044delinsCC
ENST00000697694.1:c.680_681delinsCC ENSP00000513402.1:p.Gln227Pro
ENST00000697695.1:n.1638_1639delinsCC
XM_006722001.2:c.1034_1035delinsCC XP_006722064.1:p.Gln345Pro
XM_006722001.4:c.1034_1035delinsCC XP_006722064.1:p.Gln345Pro
XM_006722002.2:c.970_971delinsCC XP_006722065.1:p.Arg324Pro
XM_006722002.4:c.970_971delinsCC XP_006722065.1:p.Arg324Pro
XM_006722004.2:c.683_684delinsCC XP_006722067.1:p.Gln228Pro
XM_006722004.3:c.683_684delinsCC XP_006722067.1:p.Gln228Pro
XM_006722005.2:c.683_684delinsCC XP_006722068.1:p.Gln228Pro
XM_006722005.3:c.683_684delinsCC XP_006722068.1:p.Gln228Pro
XM_011525092.1:c.683_684delinsCC XP_011523394.1:p.Gln228Pro
XM_011525092.2:c.683_684delinsCC XP_011523394.1:p.Gln228Pro
XM_011525093.1:c.683_684delinsCC XP_011523395.1:p.Gln228Pro
XM_011525093.2:c.683_684delinsCC XP_011523395.1:p.Gln228Pro
XM_011525094.1:c.683_684delinsCC XP_011523396.1:p.Gln228Pro
XM_011525094.2:c.683_684delinsCC XP_011523396.1:p.Gln228Pro
XM_017024914.1:c.680_681delinsCC XP_016880403.1:p.Gln227Pro
XM_017024915.1:c.680_681delinsCC XP_016880404.1:p.Gln227Pro
XM_017024916.1:c.680_681delinsCC XP_016880405.1:p.Gln227Pro
XM_017024917.1:c.680_681delinsCC XP_016880406.1:p.Gln227Pro
XM_017024918.2:c.680_681delinsCC XP_016880407.1:p.Gln227Pro
XM_017024919.1:c.619_620delinsCC XP_016880408.1:p.Arg207Pro
XR_934513.1:n.1249_1250delinsCC
XR_934513.3:n.1680_1681delinsCC
XR_934514.1:n.1252_1253delinsCC
XR_934514.3:n.1683_1684delinsCC
XR_934886.1:n.149+3948_149+3949delinsGG
XR_934886.2:n.149+3948_149+3949delinsGG