Canonical Allele Identifier: CA3261180233
Community Standard Title: NM_058216.3(RAD51C):c.1064_1065delinsAC (p.Cys355Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734155_58734156delinsAC , CM000679.2:g.58734155_58734156delinsAC GRCh38
NC_000017.10:g.56811516_56811517delinsAC , CM000679.1:g.56811516_56811517delinsAC GRCh37
NC_000017.9:g.54166515_54166516delinsAC NCBI36
NG_023199.1:g.46554_46555delinsAC , LRG_314:g.46554_46555delinsAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1064_1065delinsAC MANE Select NP_478123.1:p.Cys355Tyr
ENST00000337432.9:c.1064_1065delinsAC MANE Select ENSP00000336701.4:p.Cys355Tyr
NM_058216.2:c.1064_1065delinsAC NP_478123.1:p.Cys355Tyr
NR_103872.1:n.968_969delinsAC
NR_103872.2:n.939_940delinsAC
ENST00000337432.8:c.1064_1065delinsAC ENSP00000336701.4:p.Cys355Tyr
ENST00000413590.5:c.705_706delinsAC
ENST00000461271.6:c.*1596_*1597delinsAC ENSP00000464056.2:n.*1596_*1597delinsAC
ENST00000461706.1:n.251_252delinsAC
ENST00000475762.5:c.*1700_*1701delinsAC ENSP00000432421.1:n.*1700_*1701delinsAC
ENST00000482007.5:c.*492_*493delinsAC ENSP00000433332.1:n.*492_*493delinsAC
ENST00000487525.5:c.*640_*641delinsAC ENSP00000431637.1:n.*640_*641delinsAC
ENST00000578151.1:n.277_278delinsAC
ENST00000581221.5:n.579_580delinsAC
ENST00000584804.1:c.298_299delinsAC ENSP00000463658.1:p.Val100Thr
ENST00000697680.1:c.*2028_*2029delinsAC ENSP00000513392.1:n.*2028_*2029delinsAC
ENST00000697681.1:c.*2225_*2226delinsAC ENSP00000513393.1:n.*2225_*2226delinsAC
ENST00000697683.1:c.*2000_*2001delinsAC ENSP00000513395.1:n.*2000_*2001delinsAC
ENST00000697685.1:c.*1761_*1762delinsAC ENSP00000513396.1:n.*1761_*1762delinsAC
ENST00000697686.1:c.835_836delinsAC ENSP00000513397.1:p.Val279Thr
ENST00000697689.1:c.*1478_*1479delinsAC ENSP00000513398.1:n.*1478_*1479delinsAC
ENST00000697690.1:c.*24_*25delinsAC ENSP00000513399.1:n.*24_*25delinsAC
ENST00000697691.1:c.*1036_*1037delinsAC ENSP00000513400.1:n.*1036_*1037delinsAC
ENST00000697692.1:c.*1076_*1077delinsAC ENSP00000513401.1:n.*1076_*1077delinsAC
ENST00000697694.1:c.713_714delinsAC ENSP00000513402.1:p.Cys238Tyr
ENST00000697695.1:n.1671_1672delinsAC
XM_006722001.2:c.1067_1068delinsAC XP_006722064.1:p.Cys356Tyr
XM_006722001.4:c.1067_1068delinsAC XP_006722064.1:p.Cys356Tyr
XM_006722002.2:c.1003_1004delinsAC XP_006722065.1:p.Val335Thr
XM_006722002.4:c.1003_1004delinsAC XP_006722065.1:p.Val335Thr
XM_006722004.2:c.716_717delinsAC XP_006722067.1:p.Cys239Tyr
XM_006722004.3:c.716_717delinsAC XP_006722067.1:p.Cys239Tyr
XM_006722005.2:c.716_717delinsAC XP_006722068.1:p.Cys239Tyr
XM_006722005.3:c.716_717delinsAC XP_006722068.1:p.Cys239Tyr
XM_011525092.1:c.716_717delinsAC XP_011523394.1:p.Cys239Tyr
XM_011525092.2:c.716_717delinsAC XP_011523394.1:p.Cys239Tyr
XM_011525093.1:c.716_717delinsAC XP_011523395.1:p.Cys239Tyr
XM_011525093.2:c.716_717delinsAC XP_011523395.1:p.Cys239Tyr
XM_011525094.1:c.716_717delinsAC XP_011523396.1:p.Cys239Tyr
XM_011525094.2:c.716_717delinsAC XP_011523396.1:p.Cys239Tyr
XM_017024914.1:c.713_714delinsAC XP_016880403.1:p.Cys238Tyr
XM_017024915.1:c.713_714delinsAC XP_016880404.1:p.Cys238Tyr
XM_017024916.1:c.713_714delinsAC XP_016880405.1:p.Cys238Tyr
XM_017024917.1:c.713_714delinsAC XP_016880406.1:p.Cys238Tyr
XM_017024918.2:c.713_714delinsAC XP_016880407.1:p.Cys238Tyr
XM_017024919.1:c.652_653delinsAC XP_016880408.1:p.Val218Thr
XR_934513.1:n.1282_1283delinsAC
XR_934513.3:n.1713_1714delinsAC
XR_934514.1:n.1285_1286delinsAC
XR_934514.3:n.1716_1717delinsAC
XR_934886.1:n.149+3915_149+3916delinsGT
XR_934886.2:n.149+3915_149+3916delinsGT