Canonical Allele Identifier: CA3261179488
Community Standard Title: NM_058216.3(RAD51C):c.635_636delinsAT (p.Arg212His)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703259_58703260delinsAT , CM000679.2:g.58703259_58703260delinsAT GRCh38
NC_000017.10:g.56780620_56780621delinsAT , CM000679.1:g.56780620_56780621delinsAT GRCh37
NC_000017.9:g.54135619_54135620delinsAT NCBI36
NG_023199.1:g.15658_15659delinsAT , LRG_314:g.15658_15659delinsAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.635_636delinsAT MANE Select NP_478123.1:p.Arg212His
ENST00000337432.9:c.635_636delinsAT MANE Select ENSP00000336701.4:p.Arg212His
NM_058216.2:c.635_636delinsAT NP_478123.1:p.Arg212His
NR_103872.1:n.539_540delinsAT
NR_103872.2:n.510_511delinsAT
ENST00000337432.8:c.635_636delinsAT ENSP00000336701.4:p.Arg212His
ENST00000413590.5:c.273_274delinsAT
ENST00000425173.5:c.431_432delinsAT ENSP00000407282.1:p.Arg144His
ENST00000461271.5:c.284_285delinsAT ENSP00000464056.1:p.Arg95His
ENST00000461271.6:c.284_285delinsAT ENSP00000464056.2:p.Arg95His
ENST00000475762.5:c.*1338_*1339delinsAT ENSP00000432421.1:n.*1338_*1339delinsAT
ENST00000482007.5:c.*63_*64delinsAT ENSP00000433332.1:n.*63_*64delinsAT
ENST00000487525.5:c.*63_*64delinsAT ENSP00000431637.1:n.*63_*64delinsAT
ENST00000487921.5:n.547_548delinsAT
ENST00000583539.5:c.635_636delinsAT ENSP00000463121.1:p.Arg212His
ENST00000584617.5:c.357_358delinsAT
ENST00000697677.1:n.1716_1717delinsAT
ENST00000697678.1:n.537_538delinsAT
ENST00000697679.1:n.1709_1710delinsAT
ENST00000697680.1:c.*1499_*1500delinsAT ENSP00000513392.1:n.*1499_*1500delinsAT
ENST00000697681.1:c.*1651_*1652delinsAT ENSP00000513393.1:n.*1651_*1652delinsAT
ENST00000697683.1:c.*1499_*1500delinsAT ENSP00000513395.1:n.*1499_*1500delinsAT
ENST00000697684.1:n.695_696delinsAT
ENST00000697685.1:c.*1332_*1333delinsAT ENSP00000513396.1:n.*1332_*1333delinsAT
ENST00000697686.1:c.284_285delinsAT ENSP00000513397.1:p.Arg95His
ENST00000697687.1:n.514_515delinsAT
ENST00000697688.1:n.681_682delinsAT
ENST00000697689.1:c.*1171_*1172delinsAT ENSP00000513398.1:n.*1171_*1172delinsAT
ENST00000697690.1:c.635_636delinsAT ENSP00000513399.1:p.Arg212His
ENST00000697691.1:c.*607_*608delinsAT ENSP00000513400.1:n.*607_*608delinsAT
ENST00000697692.1:c.*647_*648delinsAT ENSP00000513401.1:n.*647_*648delinsAT
ENST00000697694.1:c.284_285delinsAT ENSP00000513402.1:p.Arg95His
ENST00000697695.1:n.1242_1243delinsAT
XM_006722001.2:c.635_636delinsAT XP_006722064.1:p.Arg212His
XM_006722001.4:c.635_636delinsAT XP_006722064.1:p.Arg212His
XM_006722002.2:c.635_636delinsAT XP_006722065.1:p.Arg212His
XM_006722002.4:c.635_636delinsAT XP_006722065.1:p.Arg212His
XM_006722004.2:c.284_285delinsAT XP_006722067.1:p.Arg95His
XM_006722004.3:c.284_285delinsAT XP_006722067.1:p.Arg95His
XM_006722005.2:c.284_285delinsAT XP_006722068.1:p.Arg95His
XM_006722005.3:c.284_285delinsAT XP_006722068.1:p.Arg95His
XM_011525092.1:c.284_285delinsAT XP_011523394.1:p.Arg95His
XM_011525092.2:c.284_285delinsAT XP_011523394.1:p.Arg95His
XM_011525093.1:c.284_285delinsAT XP_011523395.1:p.Arg95His
XM_011525093.2:c.284_285delinsAT XP_011523395.1:p.Arg95His
XM_011525094.1:c.284_285delinsAT XP_011523396.1:p.Arg95His
XM_011525094.2:c.284_285delinsAT XP_011523396.1:p.Arg95His
XM_017024914.1:c.284_285delinsAT XP_016880403.1:p.Arg95His
XM_017024915.1:c.284_285delinsAT XP_016880404.1:p.Arg95His
XM_017024916.1:c.284_285delinsAT XP_016880405.1:p.Arg95His
XM_017024917.1:c.284_285delinsAT XP_016880406.1:p.Arg95His
XM_017024918.2:c.284_285delinsAT XP_016880407.1:p.Arg95His
XM_017024919.1:c.284_285delinsAT XP_016880408.1:p.Arg95His
XR_934513.1:n.708_709delinsAT
XR_934513.3:n.1139_1140delinsAT
XR_934514.1:n.708_709delinsAT
XR_934514.3:n.1139_1140delinsAT