Canonical Allele Identifier: CA3261181292
Community Standard Title: NM_058216.3(RAD51C):c.532_534delinsAGA (p.Gln178Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696820_58696822delinsAGA , CM000679.2:g.58696820_58696822delinsAGA GRCh38
NC_000017.10:g.56774181_56774183delinsAGA , CM000679.1:g.56774181_56774183delinsAGA GRCh37
NC_000017.9:g.54129180_54129182delinsAGA NCBI36
NG_023199.1:g.9219_9221delinsAGA , LRG_314:g.9219_9221delinsAGA
NG_047169.1:g.258_260delinsTCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.532_534delinsAGA MANE Select NP_478123.1:p.Gln178Arg
ENST00000337432.9:c.532_534delinsAGA MANE Select ENSP00000336701.4:p.Gln178Arg
NM_058216.2:c.532_534delinsAGA NP_478123.1:p.Gln178Arg
NR_103872.1:n.475+1631_475+1633delinsAGA
NR_103872.2:n.446+1631_446+1633delinsAGA
ENST00000337432.8:c.532_534delinsAGA ENSP00000336701.4:p.Gln178Arg
ENST00000413590.5:c.170_172delinsAGA
ENST00000425173.5:c.328_330delinsAGA ENSP00000407282.1:p.Gln110Arg
ENST00000461271.5:c.181_183delinsAGA ENSP00000464056.1:p.Gln61Arg
ENST00000461271.6:c.181_183delinsAGA ENSP00000464056.2:p.Gln61Arg
ENST00000475762.5:c.*1235_*1237delinsAGA ENSP00000432421.1:n.*1235_*1237delinsAGA
ENST00000482007.5:c.404+1631_404+1633delinsAGA ENSP00000433332.1:n.404+1631_404+1633delinsAGA
ENST00000487525.5:c.404+1631_404+1633delinsAGA ENSP00000431637.1:n.404+1631_404+1633delinsAGA
ENST00000487921.5:n.444_446delinsAGA
ENST00000583539.5:c.532_534delinsAGA ENSP00000463121.1:p.Gln178Arg
ENST00000584617.5:c.254_256delinsAGA
ENST00000622327.4:c.268_270delinsAGA ENSP00000482326.1:p.Gln90Arg
ENST00000697675.1:n.3129_3131delinsAGA
ENST00000697676.1:n.592_594delinsAGA
ENST00000697677.1:n.1613_1615delinsAGA
ENST00000697678.1:n.434_436delinsAGA
ENST00000697679.1:n.1606_1608delinsAGA
ENST00000697680.1:c.*1396_*1398delinsAGA ENSP00000513392.1:n.*1396_*1398delinsAGA
ENST00000697681.1:c.*1423_*1425delinsAGA ENSP00000513393.1:n.*1423_*1425delinsAGA
ENST00000697683.1:c.*1396_*1398delinsAGA ENSP00000513395.1:n.*1396_*1398delinsAGA
ENST00000697684.1:n.592_594delinsAGA
ENST00000697685.1:c.*1268+1631_*1268+1633delinsAGA ENSP00000513396.1:n.*1268+1631_*1268+1633delinsAGA
ENST00000697686.1:c.181_183delinsAGA ENSP00000513397.1:p.Gln61Arg
ENST00000697687.1:n.450+1631_450+1633delinsAGA
ENST00000697688.1:n.578_580delinsAGA
ENST00000697689.1:c.*1107+1631_*1107+1633delinsAGA ENSP00000513398.1:n.*1107+1631_*1107+1633delinsAGA
ENST00000697690.1:c.532_534delinsAGA ENSP00000513399.1:p.Gln178Arg
ENST00000697691.1:c.*504_*506delinsAGA ENSP00000513400.1:n.*504_*506delinsAGA
ENST00000697692.1:c.*544_*546delinsAGA ENSP00000513401.1:n.*544_*546delinsAGA
ENST00000697694.1:c.181_183delinsAGA ENSP00000513402.1:p.Gln61Arg
ENST00000697695.1:n.1139_1141delinsAGA
XM_006722001.2:c.532_534delinsAGA XP_006722064.1:p.Gln178Arg
XM_006722001.4:c.532_534delinsAGA XP_006722064.1:p.Gln178Arg
XM_006722002.2:c.532_534delinsAGA XP_006722065.1:p.Gln178Arg
XM_006722002.4:c.532_534delinsAGA XP_006722065.1:p.Gln178Arg
XM_006722004.2:c.181_183delinsAGA XP_006722067.1:p.Gln61Arg
XM_006722004.3:c.181_183delinsAGA XP_006722067.1:p.Gln61Arg
XM_006722005.2:c.181_183delinsAGA XP_006722068.1:p.Gln61Arg
XM_006722005.3:c.181_183delinsAGA XP_006722068.1:p.Gln61Arg
XM_011525092.1:c.181_183delinsAGA XP_011523394.1:p.Gln61Arg
XM_011525092.2:c.181_183delinsAGA XP_011523394.1:p.Gln61Arg
XM_011525093.1:c.181_183delinsAGA XP_011523395.1:p.Gln61Arg
XM_011525093.2:c.181_183delinsAGA XP_011523395.1:p.Gln61Arg
XM_011525094.1:c.181_183delinsAGA XP_011523396.1:p.Gln61Arg
XM_011525094.2:c.181_183delinsAGA XP_011523396.1:p.Gln61Arg
XM_017024914.1:c.181_183delinsAGA XP_016880403.1:p.Gln61Arg
XM_017024915.1:c.181_183delinsAGA XP_016880404.1:p.Gln61Arg
XM_017024916.1:c.181_183delinsAGA XP_016880405.1:p.Gln61Arg
XM_017024917.1:c.181_183delinsAGA XP_016880406.1:p.Gln61Arg
XM_017024918.2:c.181_183delinsAGA XP_016880407.1:p.Gln61Arg
XM_017024919.1:c.181_183delinsAGA XP_016880408.1:p.Gln61Arg
XR_934513.1:n.605_607delinsAGA
XR_934513.3:n.1036_1038delinsAGA
XR_934514.1:n.605_607delinsAGA
XR_934514.3:n.1036_1038delinsAGA