Canonical Allele Identifier: CA3261180164
Community Standard Title: NM_058216.3(RAD51C):c.805_807delinsCTC (p.Met269Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709958_58709960delinsCTC , CM000679.2:g.58709958_58709960delinsCTC GRCh38
NC_000017.10:g.56787319_56787321delinsCTC , CM000679.1:g.56787319_56787321delinsCTC GRCh37
NC_000017.9:g.54142318_54142320delinsCTC NCBI36
NG_023199.1:g.22357_22359delinsCTC , LRG_314:g.22357_22359delinsCTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.805_807delinsCTC MANE Select NP_478123.1:p.Met269Leu
ENST00000337432.9:c.805_807delinsCTC MANE Select ENSP00000336701.4:p.Met269Leu
NM_058216.2:c.805_807delinsCTC NP_478123.1:p.Met269Leu
NR_103872.1:n.709_711delinsCTC
NR_103872.2:n.680_682delinsCTC
ENST00000337432.8:c.805_807delinsCTC ENSP00000336701.4:p.Met269Leu
ENST00000413590.5:c.443_445delinsCTC
ENST00000461271.6:c.454_456delinsCTC ENSP00000464056.2:p.Met152Leu
ENST00000475762.5:c.*1508_*1510delinsCTC ENSP00000432421.1:n.*1508_*1510delinsCTC
ENST00000482007.5:c.*233_*235delinsCTC ENSP00000433332.1:n.*233_*235delinsCTC
ENST00000487525.5:c.*378_*380delinsCTC ENSP00000431637.1:n.*378_*380delinsCTC
ENST00000578151.1:n.140_142delinsCTC
ENST00000581221.5:n.320_322delinsCTC
ENST00000583539.5:c.805_807delinsCTC ENSP00000463121.1:p.Met269Leu
ENST00000584617.5:c.527_529delinsCTC
ENST00000584804.1:c.100_102delinsCTC ENSP00000463658.1:p.Met34Leu
ENST00000697678.1:n.707_709delinsCTC
ENST00000697679.1:n.1879_1881delinsCTC
ENST00000697680.1:c.*1669_*1671delinsCTC ENSP00000513392.1:n.*1669_*1671delinsCTC
ENST00000697681.1:c.*1966_*1968delinsCTC ENSP00000513393.1:n.*1966_*1968delinsCTC
ENST00000697683.1:c.*1669_*1671delinsCTC ENSP00000513395.1:n.*1669_*1671delinsCTC
ENST00000697684.1:n.865_867delinsCTC
ENST00000697685.1:c.*1502_*1504delinsCTC ENSP00000513396.1:n.*1502_*1504delinsCTC
ENST00000697686.1:c.454_456delinsCTC ENSP00000513397.1:p.Met152Leu
ENST00000697687.1:n.684_686delinsCTC
ENST00000697688.1:n.851_853delinsCTC
ENST00000697689.1:c.*1341_*1343delinsCTC ENSP00000513398.1:n.*1341_*1343delinsCTC
ENST00000697690.1:c.805_807delinsCTC ENSP00000513399.1:p.Met269Leu
ENST00000697691.1:c.*777_*779delinsCTC ENSP00000513400.1:n.*777_*779delinsCTC
ENST00000697692.1:c.*817_*819delinsCTC ENSP00000513401.1:n.*817_*819delinsCTC
ENST00000697694.1:c.454_456delinsCTC ENSP00000513402.1:p.Met152Leu
ENST00000697695.1:n.1412_1414delinsCTC
XM_006722001.2:c.805_807delinsCTC XP_006722064.1:p.Met269Leu
XM_006722001.4:c.805_807delinsCTC XP_006722064.1:p.Met269Leu
XM_006722002.2:c.805_807delinsCTC XP_006722065.1:p.Met269Leu
XM_006722002.4:c.805_807delinsCTC XP_006722065.1:p.Met269Leu
XM_006722004.2:c.454_456delinsCTC XP_006722067.1:p.Met152Leu
XM_006722004.3:c.454_456delinsCTC XP_006722067.1:p.Met152Leu
XM_006722005.2:c.454_456delinsCTC XP_006722068.1:p.Met152Leu
XM_006722005.3:c.454_456delinsCTC XP_006722068.1:p.Met152Leu
XM_011525092.1:c.454_456delinsCTC XP_011523394.1:p.Met152Leu
XM_011525092.2:c.454_456delinsCTC XP_011523394.1:p.Met152Leu
XM_011525093.1:c.454_456delinsCTC XP_011523395.1:p.Met152Leu
XM_011525093.2:c.454_456delinsCTC XP_011523395.1:p.Met152Leu
XM_011525094.1:c.454_456delinsCTC XP_011523396.1:p.Met152Leu
XM_011525094.2:c.454_456delinsCTC XP_011523396.1:p.Met152Leu
XM_017024914.1:c.454_456delinsCTC XP_016880403.1:p.Met152Leu
XM_017024915.1:c.454_456delinsCTC XP_016880404.1:p.Met152Leu
XM_017024916.1:c.454_456delinsCTC XP_016880405.1:p.Met152Leu
XM_017024917.1:c.454_456delinsCTC XP_016880406.1:p.Met152Leu
XM_017024918.2:c.454_456delinsCTC XP_016880407.1:p.Met152Leu
XM_017024919.1:c.454_456delinsCTC XP_016880408.1:p.Met152Leu
XR_934513.1:n.1023_1025delinsCTC
XR_934513.3:n.1454_1456delinsCTC
XR_934514.1:n.1023_1025delinsCTC
XR_934514.3:n.1454_1456delinsCTC