Canonical Allele Identifier: CA3261178556
Community Standard Title: NM_058216.3(RAD51C):c.4_6delinsGGA (p.Arg2Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692647_58692649delinsGGA , CM000679.2:g.58692647_58692649delinsGGA GRCh38
NC_000017.10:g.56770008_56770010delinsGGA , CM000679.1:g.56770008_56770010delinsGGA GRCh37
NC_000017.9:g.54125007_54125009delinsGGA NCBI36
NG_023199.1:g.5046_5048delinsGGA , LRG_314:g.5046_5048delinsGGA
NG_047169.1:g.4431_4433delinsTCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.4_6delinsGGA MANE Select NP_478123.1:p.Arg2Gly
ENST00000337432.9:c.4_6delinsGGA MANE Select ENSP00000336701.4:p.Arg2Gly
NM_002876.3:c.4_6delinsGGA NP_002867.1:p.Arg2Gly
NM_002876.4:c.4_6delinsGGA NP_002867.1:p.Arg2Gly
NM_058216.2:c.4_6delinsGGA NP_478123.1:p.Arg2Gly
NR_103872.1:n.75_77delinsGGA
NR_103872.2:n.46_48delinsGGA
NR_103873.1:n.75_77delinsGGA
ENST00000337432.8:c.4_6delinsGGA ENSP00000336701.4:p.Arg2Gly
ENST00000421782.3:c.4_6delinsGGA ENSP00000391450.2:p.Arg2Gly
ENST00000461271.5:c.-245_-243delinsGGA ENSP00000464056.1:n.-245_-243delinsGGA
ENST00000461271.6:c.-245_-243delinsGGA ENSP00000464056.2:n.-245_-243delinsGGA
ENST00000475762.5:c.4_6delinsGGA ENSP00000432421.1:p.Arg2Gly
ENST00000476741.2:n.46_48delinsGGA
ENST00000482007.5:c.4_6delinsGGA ENSP00000433332.1:p.Arg2Gly
ENST00000486827.1:c.4_6delinsGGA ENSP00000436761.1:p.Arg2Gly
ENST00000487525.5:c.4_6delinsGGA ENSP00000431637.1:p.Arg2Gly
ENST00000487921.5:n.57+15_57+17delinsGGA
ENST00000583539.5:c.4_6delinsGGA ENSP00000463121.1:p.Arg2Gly
ENST00000697675.1:n.75_77delinsGGA
ENST00000697676.1:n.64_66delinsGGA
ENST00000697677.1:n.62_64delinsGGA
ENST00000697678.1:n.47+15_47+17delinsGGA
ENST00000697679.1:n.55_57delinsGGA
ENST00000697680.1:c.4_6delinsGGA ENSP00000513392.1:p.Arg2Gly
ENST00000697681.1:c.4_6delinsGGA ENSP00000513393.1:p.Arg2Gly
ENST00000697683.1:c.4_6delinsGGA ENSP00000513395.1:p.Arg2Gly
ENST00000697684.1:n.64_66delinsGGA
ENST00000697685.1:c.4_6delinsGGA ENSP00000513396.1:p.Arg2Gly
ENST00000697686.1:c.-207+15_-207+17delinsGGA ENSP00000513397.1:n.-207+15_-207+17delinsGGA
ENST00000697687.1:n.50_52delinsGGA
ENST00000697688.1:n.50_52delinsGGA
ENST00000697689.1:c.4_6delinsGGA ENSP00000513398.1:p.Arg2Gly
ENST00000697690.1:c.4_6delinsGGA ENSP00000513399.1:p.Arg2Gly
ENST00000697691.1:c.4_6delinsGGA ENSP00000513400.1:p.Arg2Gly
ENST00000697692.1:c.4_6delinsGGA ENSP00000513401.1:p.Arg2Gly
XM_006722001.2:c.4_6delinsGGA XP_006722064.1:p.Arg2Gly
XM_006722001.4:c.4_6delinsGGA XP_006722064.1:p.Arg2Gly
XM_006722002.2:c.4_6delinsGGA XP_006722065.1:p.Arg2Gly
XM_006722002.4:c.4_6delinsGGA XP_006722065.1:p.Arg2Gly
XM_006722004.2:c.-245_-243delinsGGA XP_006722067.1:n.-245_-243delinsGGA
XM_006722004.3:c.-245_-243delinsGGA XP_006722067.1:n.-245_-243delinsGGA
XM_006722005.2:c.-207+15_-207+17delinsGGA XP_006722068.1:n.-207+15_-207+17delinsGGA
XM_006722005.3:c.-207+15_-207+17delinsGGA XP_006722068.1:n.-207+15_-207+17delinsGGA
XM_011525092.1:c.-545_-543delinsGGA XP_011523394.1:n.-545_-543delinsGGA
XM_011525093.1:c.-706_-704delinsGGA XP_011523395.1:n.-706_-704delinsGGA
XM_017024914.1:c.-245_-243delinsGGA XP_016880403.1:n.-245_-243delinsGGA
XM_017024916.1:c.-545_-543delinsGGA XP_016880405.1:n.-545_-543delinsGGA
XM_017024917.1:c.-207+15_-207+17delinsGGA XP_016880406.1:n.-207+15_-207+17delinsGGA
XM_017024918.2:c.-519_-517delinsGGA XP_016880407.1:n.-519_-517delinsGGA
XR_934513.1:n.77_79delinsGGA
XR_934513.3:n.508_510delinsGGA
XR_934514.1:n.77_79delinsGGA
XR_934514.3:n.508_510delinsGGA