Canonical Allele Identifier: CA3261180041
Community Standard Title: NM_058216.3(RAD51C):c.1055_1056delinsAC (p.Thr352Asn)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734146_58734147delinsAC , CM000679.2:g.58734146_58734147delinsAC GRCh38
NC_000017.10:g.56811507_56811508delinsAC , CM000679.1:g.56811507_56811508delinsAC GRCh37
NC_000017.9:g.54166506_54166507delinsAC NCBI36
NG_023199.1:g.46545_46546delinsAC , LRG_314:g.46545_46546delinsAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1055_1056delinsAC MANE Select NP_478123.1:p.Thr352Asn
ENST00000337432.9:c.1055_1056delinsAC MANE Select ENSP00000336701.4:p.Thr352Asn
NM_058216.2:c.1055_1056delinsAC NP_478123.1:p.Thr352Asn
NR_103872.1:n.959_960delinsAC
NR_103872.2:n.930_931delinsAC
ENST00000337432.8:c.1055_1056delinsAC ENSP00000336701.4:p.Thr352Asn
ENST00000413590.5:c.696_697delinsAC
ENST00000461271.6:c.*1587_*1588delinsAC ENSP00000464056.2:n.*1587_*1588delinsAC
ENST00000461706.1:n.242_243delinsAC
ENST00000475762.5:c.*1691_*1692delinsAC ENSP00000432421.1:n.*1691_*1692delinsAC
ENST00000482007.5:c.*483_*484delinsAC ENSP00000433332.1:n.*483_*484delinsAC
ENST00000487525.5:c.*631_*632delinsAC ENSP00000431637.1:n.*631_*632delinsAC
ENST00000578151.1:n.268_269delinsAC
ENST00000581221.5:n.570_571delinsAC
ENST00000584804.1:c.289_290delinsAC ENSP00000463658.1:p.Leu97Thr
ENST00000697680.1:c.*2019_*2020delinsAC ENSP00000513392.1:n.*2019_*2020delinsAC
ENST00000697681.1:c.*2216_*2217delinsAC ENSP00000513393.1:n.*2216_*2217delinsAC
ENST00000697683.1:c.*1991_*1992delinsAC ENSP00000513395.1:n.*1991_*1992delinsAC
ENST00000697685.1:c.*1752_*1753delinsAC ENSP00000513396.1:n.*1752_*1753delinsAC
ENST00000697686.1:c.826_827delinsAC ENSP00000513397.1:p.Leu276Thr
ENST00000697689.1:c.*1469_*1470delinsAC ENSP00000513398.1:n.*1469_*1470delinsAC
ENST00000697690.1:c.*15_*16delinsAC ENSP00000513399.1:n.*15_*16delinsAC
ENST00000697691.1:c.*1027_*1028delinsAC ENSP00000513400.1:n.*1027_*1028delinsAC
ENST00000697692.1:c.*1067_*1068delinsAC ENSP00000513401.1:n.*1067_*1068delinsAC
ENST00000697694.1:c.704_705delinsAC ENSP00000513402.1:p.Thr235Asn
ENST00000697695.1:n.1662_1663delinsAC
XM_006722001.2:c.1058_1059delinsAC XP_006722064.1:p.Thr353Asn
XM_006722001.4:c.1058_1059delinsAC XP_006722064.1:p.Thr353Asn
XM_006722002.2:c.994_995delinsAC XP_006722065.1:p.Leu332Thr
XM_006722002.4:c.994_995delinsAC XP_006722065.1:p.Leu332Thr
XM_006722004.2:c.707_708delinsAC XP_006722067.1:p.Thr236Asn
XM_006722004.3:c.707_708delinsAC XP_006722067.1:p.Thr236Asn
XM_006722005.2:c.707_708delinsAC XP_006722068.1:p.Thr236Asn
XM_006722005.3:c.707_708delinsAC XP_006722068.1:p.Thr236Asn
XM_011525092.1:c.707_708delinsAC XP_011523394.1:p.Thr236Asn
XM_011525092.2:c.707_708delinsAC XP_011523394.1:p.Thr236Asn
XM_011525093.1:c.707_708delinsAC XP_011523395.1:p.Thr236Asn
XM_011525093.2:c.707_708delinsAC XP_011523395.1:p.Thr236Asn
XM_011525094.1:c.707_708delinsAC XP_011523396.1:p.Thr236Asn
XM_011525094.2:c.707_708delinsAC XP_011523396.1:p.Thr236Asn
XM_017024914.1:c.704_705delinsAC XP_016880403.1:p.Thr235Asn
XM_017024915.1:c.704_705delinsAC XP_016880404.1:p.Thr235Asn
XM_017024916.1:c.704_705delinsAC XP_016880405.1:p.Thr235Asn
XM_017024917.1:c.704_705delinsAC XP_016880406.1:p.Thr235Asn
XM_017024918.2:c.704_705delinsAC XP_016880407.1:p.Thr235Asn
XM_017024919.1:c.643_644delinsAC XP_016880408.1:p.Leu215Thr
XR_934513.1:n.1273_1274delinsAC
XR_934513.3:n.1704_1705delinsAC
XR_934514.1:n.1276_1277delinsAC
XR_934514.3:n.1707_1708delinsAC
XR_934886.1:n.149+3924_149+3925delinsGT
XR_934886.2:n.149+3924_149+3925delinsGT