Canonical Allele Identifier: CA3057228115

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692649_58692650delinsGT , CM000679.2:g.58692649_58692650delinsGT	GRCh38
NC_000017.10:g.56770010_56770011delinsGT , CM000679.1:g.56770010_56770011delinsGT	GRCh37
NC_000017.9:g.54125009_54125010delinsGT	NCBI36
NG_023199.1:g.5048_5049delinsGT , LRG_314:g.5048_5049delinsGT
NG_047169.1:g.4430_4431delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-243_-242delinsGT	ENSP00000464056.2:n.-243_-242delinsGT
ENST00000697675.1:n.77_78delinsGT
ENST00000697676.1:n.66_67delinsGT
ENST00000697677.1:n.64_65delinsGT
ENST00000697678.1:n.47+17_47+18delinsGT
ENST00000697679.1:n.57_58delinsGT
ENST00000697680.1:c.6_7delinsGT	ENSP00000513392.1:p.Gly3Trp
ENST00000697681.1:c.6_7delinsGT	ENSP00000513393.1:p.Gly3Trp
ENST00000697683.1:c.6_7delinsGT	ENSP00000513395.1:p.Gly3Trp
ENST00000697684.1:n.66_67delinsGT
ENST00000697685.1:c.6_7delinsGT	ENSP00000513396.1:p.Gly3Trp
ENST00000697686.1:c.-207+17_-207+18delinsGT	ENSP00000513397.1:n.-207+17_-207+18delinsGT
ENST00000697687.1:n.52_53delinsGT
ENST00000697688.1:n.52_53delinsGT
ENST00000697689.1:c.6_7delinsGT	ENSP00000513398.1:p.Gly3Trp
ENST00000697690.1:c.6_7delinsGT	ENSP00000513399.1:p.Gly3Trp
ENST00000697691.1:c.6_7delinsGT	ENSP00000513400.1:p.Gly3Trp
ENST00000697692.1:c.6_7delinsGT	ENSP00000513401.1:p.Gly3Trp
ENST00000337432.9:c.6_7delinsGT MANE Select	ENSP00000336701.4:p.Gly3Trp
ENST00000337432.8:c.6_7delinsGT	ENSP00000336701.4:p.Gly3Trp
ENST00000421782.3:c.6_7delinsGT	ENSP00000391450.2:p.Gly3Trp
ENST00000461271.5:c.-243_-242delinsGT	ENSP00000464056.1:n.-243_-242delinsGT
ENST00000475762.5:c.6_7delinsGT	ENSP00000432421.1:p.Gly3Trp
ENST00000476741.2:n.48_49delinsGT
ENST00000482007.5:c.6_7delinsGT	ENSP00000433332.1:p.Gly3Trp
ENST00000486827.1:c.6_7delinsGT	ENSP00000436761.1:p.Gly3Trp
ENST00000487525.5:c.6_7delinsGT	ENSP00000431637.1:p.Gly3Trp
ENST00000487921.5:n.57+17_57+18delinsGT
ENST00000583539.5:c.6_7delinsGT	ENSP00000463121.1:p.Gly3Trp
NM_002876.3:c.6_7delinsGT	NP_002867.1:p.Gly3Trp
NM_058216.2:c.6_7delinsGT	NP_478123.1:p.Gly3Trp
NR_103872.1:n.77_78delinsGT
NR_103873.1:n.77_78delinsGT
XM_006722001.2:c.6_7delinsGT	XP_006722064.1:p.Gly3Trp
XM_006722002.2:c.6_7delinsGT	XP_006722065.1:p.Gly3Trp
XM_006722004.2:c.-243_-242delinsGT	XP_006722067.1:n.-243_-242delinsGT
XM_006722005.2:c.-207+17_-207+18delinsGT	XP_006722068.1:n.-207+17_-207+18delinsGT
XM_011525092.1:c.-543_-542delinsGT	XP_011523394.1:n.-543_-542delinsGT
XM_011525093.1:c.-704_-703delinsGT	XP_011523395.1:n.-704_-703delinsGT
XR_934513.1:n.79_80delinsGT
XR_934514.1:n.79_80delinsGT
XM_006722001.4:c.6_7delinsGT	XP_006722064.1:p.Gly3Trp
XM_006722002.4:c.6_7delinsGT	XP_006722065.1:p.Gly3Trp
XM_006722004.3:c.-243_-242delinsGT	XP_006722067.1:n.-243_-242delinsGT
XM_006722005.3:c.-207+17_-207+18delinsGT	XP_006722068.1:n.-207+17_-207+18delinsGT
XM_017024914.1:c.-243_-242delinsGT	XP_016880403.1:n.-243_-242delinsGT
XM_017024916.1:c.-543_-542delinsGT	XP_016880405.1:n.-543_-542delinsGT
XM_017024917.1:c.-207+17_-207+18delinsGT	XP_016880406.1:n.-207+17_-207+18delinsGT
XM_017024918.2:c.-517_-516delinsGT	XP_016880407.1:n.-517_-516delinsGT
XR_934513.3:n.510_511delinsGT
XR_934514.3:n.510_511delinsGT
NM_058216.3:c.6_7delinsGT MANE Select	NP_478123.1:p.Gly3Trp
NR_103872.2:n.48_49delinsGT
NM_002876.4:c.6_7delinsGT	NP_002867.1:p.Gly3Trp