Canonical Allele Identifier: CA3261178663
Community Standard Title: NM_058216.3(RAD51C):c.577_578delinsTA (p.Arg193Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703201_58703202delinsTA , CM000679.2:g.58703201_58703202delinsTA GRCh38
NC_000017.10:g.56780562_56780563delinsTA , CM000679.1:g.56780562_56780563delinsTA GRCh37
NC_000017.9:g.54135561_54135562delinsTA NCBI36
NG_023199.1:g.15600_15601delinsTA , LRG_314:g.15600_15601delinsTA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.577_578delinsTA MANE Select NP_478123.1:p.Arg193Ter
ENST00000337432.9:c.577_578delinsTA MANE Select ENSP00000336701.4:p.Arg193Ter
NM_058216.2:c.577_578delinsTA NP_478123.1:p.Arg193Ter
NR_103872.1:n.481_482delinsTA
NR_103872.2:n.452_453delinsTA
ENST00000337432.8:c.577_578delinsTA ENSP00000336701.4:p.Arg193Ter
ENST00000413590.5:c.215_216delinsTA
ENST00000425173.5:c.373_374delinsTA ENSP00000407282.1:p.Arg125Ter
ENST00000461271.5:c.226_227delinsTA ENSP00000464056.1:p.Arg76Ter
ENST00000461271.6:c.226_227delinsTA ENSP00000464056.2:p.Arg76Ter
ENST00000475762.5:c.*1280_*1281delinsTA ENSP00000432421.1:n.*1280_*1281delinsTA
ENST00000482007.5:c.*5_*6delinsTA ENSP00000433332.1:n.*5_*6delinsTA
ENST00000487525.5:c.*5_*6delinsTA ENSP00000431637.1:n.*5_*6delinsTA
ENST00000487921.5:n.489_490delinsTA
ENST00000583539.5:c.577_578delinsTA ENSP00000463121.1:p.Arg193Ter
ENST00000584617.5:c.299_300delinsTA
ENST00000697677.1:n.1658_1659delinsTA
ENST00000697678.1:n.479_480delinsTA
ENST00000697679.1:n.1651_1652delinsTA
ENST00000697680.1:c.*1441_*1442delinsTA ENSP00000513392.1:n.*1441_*1442delinsTA
ENST00000697681.1:c.*1593_*1594delinsTA ENSP00000513393.1:n.*1593_*1594delinsTA
ENST00000697683.1:c.*1441_*1442delinsTA ENSP00000513395.1:n.*1441_*1442delinsTA
ENST00000697684.1:n.637_638delinsTA
ENST00000697685.1:c.*1274_*1275delinsTA ENSP00000513396.1:n.*1274_*1275delinsTA
ENST00000697686.1:c.226_227delinsTA ENSP00000513397.1:p.Arg76Ter
ENST00000697687.1:n.456_457delinsTA
ENST00000697688.1:n.623_624delinsTA
ENST00000697689.1:c.*1113_*1114delinsTA ENSP00000513398.1:n.*1113_*1114delinsTA
ENST00000697690.1:c.577_578delinsTA ENSP00000513399.1:p.Arg193Ter
ENST00000697691.1:c.*549_*550delinsTA ENSP00000513400.1:n.*549_*550delinsTA
ENST00000697692.1:c.*589_*590delinsTA ENSP00000513401.1:n.*589_*590delinsTA
ENST00000697694.1:c.226_227delinsTA ENSP00000513402.1:p.Arg76Ter
ENST00000697695.1:n.1184_1185delinsTA
XM_006722001.2:c.577_578delinsTA XP_006722064.1:p.Arg193Ter
XM_006722001.4:c.577_578delinsTA XP_006722064.1:p.Arg193Ter
XM_006722002.2:c.577_578delinsTA XP_006722065.1:p.Arg193Ter
XM_006722002.4:c.577_578delinsTA XP_006722065.1:p.Arg193Ter
XM_006722004.2:c.226_227delinsTA XP_006722067.1:p.Arg76Ter
XM_006722004.3:c.226_227delinsTA XP_006722067.1:p.Arg76Ter
XM_006722005.2:c.226_227delinsTA XP_006722068.1:p.Arg76Ter
XM_006722005.3:c.226_227delinsTA XP_006722068.1:p.Arg76Ter
XM_011525092.1:c.226_227delinsTA XP_011523394.1:p.Arg76Ter
XM_011525092.2:c.226_227delinsTA XP_011523394.1:p.Arg76Ter
XM_011525093.1:c.226_227delinsTA XP_011523395.1:p.Arg76Ter
XM_011525093.2:c.226_227delinsTA XP_011523395.1:p.Arg76Ter
XM_011525094.1:c.226_227delinsTA XP_011523396.1:p.Arg76Ter
XM_011525094.2:c.226_227delinsTA XP_011523396.1:p.Arg76Ter
XM_017024914.1:c.226_227delinsTA XP_016880403.1:p.Arg76Ter
XM_017024915.1:c.226_227delinsTA XP_016880404.1:p.Arg76Ter
XM_017024916.1:c.226_227delinsTA XP_016880405.1:p.Arg76Ter
XM_017024917.1:c.226_227delinsTA XP_016880406.1:p.Arg76Ter
XM_017024918.2:c.226_227delinsTA XP_016880407.1:p.Arg76Ter
XM_017024919.1:c.226_227delinsTA XP_016880408.1:p.Arg76Ter
XR_934513.1:n.650_651delinsTA
XR_934513.3:n.1081_1082delinsTA
XR_934514.1:n.650_651delinsTA
XR_934514.3:n.1081_1082delinsTA