Canonical Allele Identifier: CA2638988863

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58692758-CTAGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692759_58692763del , CM000679.2:g.58692759_58692763del	GRCh38
NC_000017.10:g.56770120_56770124del , CM000679.1:g.56770120_56770124del	GRCh37
NC_000017.9:g.54125119_54125123del	NCBI36
NG_023199.1:g.5158_5162del , LRG_314:g.5158_5162del
NG_047169.1:g.4317_4321del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-207+74_-207+78del	ENSP00000464056.2:n.-207+74_-207+78del
ENST00000697675.1:n.187_191del
ENST00000697676.1:n.176_180del
ENST00000697677.1:n.174_178del
ENST00000697678.1:n.47+127_47+131del
ENST00000697679.1:n.167_171del
ENST00000697680.1:c.116_120del	ENSP00000513392.1:p.Leu39ArgfsTer7
ENST00000697681.1:c.116_120del	ENSP00000513393.1:p.Leu39ArgfsTer7
ENST00000697683.1:c.116_120del	ENSP00000513395.1:p.Leu39ArgfsTer7
ENST00000697684.1:n.176_180del
ENST00000697685.1:c.116_120del	ENSP00000513396.1:p.Leu39ArgfsTer7
ENST00000697686.1:c.-207+127_-207+131del	ENSP00000513397.1:n.-207+127_-207+131del
ENST00000697687.1:n.162_166del
ENST00000697688.1:n.162_166del
ENST00000697689.1:c.116_120del	ENSP00000513398.1:p.Leu39ArgfsTer7
ENST00000697690.1:c.116_120del	ENSP00000513399.1:p.Leu39ArgfsTer7
ENST00000697691.1:c.42+74_42+78del	ENSP00000513400.1:n.42+74_42+78del
ENST00000697692.1:c.116_120del	ENSP00000513401.1:p.Leu39ArgfsTer7
ENST00000697693.1:n.29_33del
ENST00000337432.9:c.116_120del MANE Select	ENSP00000336701.4:p.Leu39ArgfsTer7
ENST00000337432.8:c.116_120del	ENSP00000336701.4:p.Leu39ArgfsTer7
ENST00000421782.3:c.116_120del	ENSP00000391450.2:p.Leu39ArgfsTer7
ENST00000461271.5:c.-207+74_-207+78del	ENSP00000464056.1:n.-207+74_-207+78del
ENST00000475762.5:c.116_120del	ENSP00000432421.1:p.Leu39ArgfsTer7
ENST00000476741.2:n.158_162del
ENST00000482007.5:c.116_120del	ENSP00000433332.1:p.Leu39ArgfsTer7
ENST00000486827.1:c.116_120del	ENSP00000436761.1:p.Leu39ArgfsTer7
ENST00000487525.5:c.116_120del	ENSP00000431637.1:p.Leu39ArgfsTer7
ENST00000487921.5:n.57+127_57+131del
ENST00000583539.5:c.116_120del	ENSP00000463121.1:p.Leu39ArgfsTer7
ENST00000584617.5:c.97_101del
NM_002876.3:c.116_120del	NP_002867.1:p.Leu39ArgfsTer7
NM_058216.2:c.116_120del	NP_478123.1:p.Leu39ArgfsTer7
NR_103872.1:n.187_191del
NR_103873.1:n.113+74_113+78del
XM_006722001.2:c.116_120del	XP_006722064.1:p.Leu39ArgfsTer7
XM_006722002.2:c.116_120del	XP_006722065.1:p.Leu39ArgfsTer7
XM_006722004.2:c.-207+74_-207+78del	XP_006722067.1:n.-207+74_-207+78del
XM_006722005.2:c.-207+127_-207+131del	XP_006722068.1:n.-207+127_-207+131del
XM_011525092.1:c.-507+74_-507+78del	XP_011523394.1:n.-507+74_-507+78del
XM_011525093.1:c.-668+74_-668+78del	XP_011523395.1:n.-668+74_-668+78del
XR_934513.1:n.189_193del
XR_934514.1:n.189_193del
XM_006722001.4:c.116_120del	XP_006722064.1:p.Leu39ArgfsTer7
XM_006722002.4:c.116_120del	XP_006722065.1:p.Leu39ArgfsTer7
XM_006722004.3:c.-207+74_-207+78del	XP_006722067.1:n.-207+74_-207+78del
XM_006722005.3:c.-207+127_-207+131del	XP_006722068.1:n.-207+127_-207+131del
XM_011525092.2:c.-507+74_-507+78del	XP_011523394.1:n.-507+74_-507+78del
XM_011525093.2:c.-668+74_-668+78del	XP_011523395.1:n.-668+74_-668+78del
XM_017024914.1:c.-207+74_-207+78del	XP_016880403.1:n.-207+74_-207+78del
XM_017024916.1:c.-507+74_-507+78del	XP_016880405.1:n.-507+74_-507+78del
XM_017024917.1:c.-207+127_-207+131del	XP_016880406.1:n.-207+127_-207+131del
XM_017024918.2:c.-407_-403del	XP_016880407.1:n.-407_-403del
XM_017024919.1:c.-668+74_-668+78del	XP_016880408.1:n.-668+74_-668+78del
XR_934513.3:n.620_624del
XR_934514.3:n.620_624del
NM_058216.3:c.116_120del MANE Select	NP_478123.1:p.Leu39ArgfsTer7
NR_103872.2:n.158_162del
NM_002876.4:c.116_120del	NP_002867.1:p.Leu39ArgfsTer7