Canonical Allele Identifier: CA3261179619
Community Standard Title: NM_058216.3(RAD51C):c.1031_1032delinsTC (p.Gln344Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734122_58734123delinsTC , CM000679.2:g.58734122_58734123delinsTC GRCh38
NC_000017.10:g.56811483_56811484delinsTC , CM000679.1:g.56811483_56811484delinsTC GRCh37
NC_000017.9:g.54166482_54166483delinsTC NCBI36
NG_023199.1:g.46521_46522delinsTC , LRG_314:g.46521_46522delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1031_1032delinsTC MANE Select NP_478123.1:p.Gln344Leu
ENST00000337432.9:c.1031_1032delinsTC MANE Select ENSP00000336701.4:p.Gln344Leu
NM_058216.2:c.1031_1032delinsTC NP_478123.1:p.Gln344Leu
NR_103872.1:n.935_936delinsTC
NR_103872.2:n.906_907delinsTC
ENST00000337432.8:c.1031_1032delinsTC ENSP00000336701.4:p.Gln344Leu
ENST00000413590.5:c.672_673delinsTC
ENST00000461271.6:c.*1563_*1564delinsTC ENSP00000464056.2:n.*1563_*1564delinsTC
ENST00000461706.1:n.218_219delinsTC
ENST00000475762.5:c.*1667_*1668delinsTC ENSP00000432421.1:n.*1667_*1668delinsTC
ENST00000482007.5:c.*459_*460delinsTC ENSP00000433332.1:n.*459_*460delinsTC
ENST00000487525.5:c.*607_*608delinsTC ENSP00000431637.1:n.*607_*608delinsTC
ENST00000578151.1:n.244_245delinsTC
ENST00000581221.5:n.546_547delinsTC
ENST00000584804.1:c.265_266delinsTC ENSP00000463658.1:p.Arg89Ser
ENST00000697680.1:c.*1995_*1996delinsTC ENSP00000513392.1:n.*1995_*1996delinsTC
ENST00000697681.1:c.*2192_*2193delinsTC ENSP00000513393.1:n.*2192_*2193delinsTC
ENST00000697683.1:c.*1967_*1968delinsTC ENSP00000513395.1:n.*1967_*1968delinsTC
ENST00000697685.1:c.*1728_*1729delinsTC ENSP00000513396.1:n.*1728_*1729delinsTC
ENST00000697686.1:c.802_803delinsTC ENSP00000513397.1:p.Arg268Ser
ENST00000697689.1:c.*1445_*1446delinsTC ENSP00000513398.1:n.*1445_*1446delinsTC
ENST00000697690.1:c.909_910delinsTC ENSP00000513399.1:p.Gly304Arg
ENST00000697691.1:c.*1003_*1004delinsTC ENSP00000513400.1:n.*1003_*1004delinsTC
ENST00000697692.1:c.*1043_*1044delinsTC ENSP00000513401.1:n.*1043_*1044delinsTC
ENST00000697694.1:c.680_681delinsTC ENSP00000513402.1:p.Gln227Leu
ENST00000697695.1:n.1638_1639delinsTC
XM_006722001.2:c.1034_1035delinsTC XP_006722064.1:p.Gln345Leu
XM_006722001.4:c.1034_1035delinsTC XP_006722064.1:p.Gln345Leu
XM_006722002.2:c.970_971delinsTC XP_006722065.1:p.Arg324Ser
XM_006722002.4:c.970_971delinsTC XP_006722065.1:p.Arg324Ser
XM_006722004.2:c.683_684delinsTC XP_006722067.1:p.Gln228Leu
XM_006722004.3:c.683_684delinsTC XP_006722067.1:p.Gln228Leu
XM_006722005.2:c.683_684delinsTC XP_006722068.1:p.Gln228Leu
XM_006722005.3:c.683_684delinsTC XP_006722068.1:p.Gln228Leu
XM_011525092.1:c.683_684delinsTC XP_011523394.1:p.Gln228Leu
XM_011525092.2:c.683_684delinsTC XP_011523394.1:p.Gln228Leu
XM_011525093.1:c.683_684delinsTC XP_011523395.1:p.Gln228Leu
XM_011525093.2:c.683_684delinsTC XP_011523395.1:p.Gln228Leu
XM_011525094.1:c.683_684delinsTC XP_011523396.1:p.Gln228Leu
XM_011525094.2:c.683_684delinsTC XP_011523396.1:p.Gln228Leu
XM_017024914.1:c.680_681delinsTC XP_016880403.1:p.Gln227Leu
XM_017024915.1:c.680_681delinsTC XP_016880404.1:p.Gln227Leu
XM_017024916.1:c.680_681delinsTC XP_016880405.1:p.Gln227Leu
XM_017024917.1:c.680_681delinsTC XP_016880406.1:p.Gln227Leu
XM_017024918.2:c.680_681delinsTC XP_016880407.1:p.Gln227Leu
XM_017024919.1:c.619_620delinsTC XP_016880408.1:p.Arg207Ser
XR_934513.1:n.1249_1250delinsTC
XR_934513.3:n.1680_1681delinsTC
XR_934514.1:n.1252_1253delinsTC
XR_934514.3:n.1683_1684delinsTC
XR_934886.1:n.149+3948_149+3949delinsGA
XR_934886.2:n.149+3948_149+3949delinsGA