Canonical Allele Identifier: CA400340035

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694991T>C , CM000679.2:g.58694991T>C	GRCh38
NC_000017.10:g.56772352T>C , CM000679.1:g.56772352T>C	GRCh37
NC_000017.9:g.54127351T>C	NCBI36
NG_023199.1:g.7390T>C , LRG_314:g.7390T>C
NG_047169.1:g.2089A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.206T>C MANE Select	NP_478123.1:p.Leu69Pro
ENST00000337432.9:c.206T>C MANE Select	ENSP00000336701.4:p.Leu69Pro
NM_002876.3:c.206T>C	NP_002867.1:p.Leu69Pro
NM_002876.4:c.206T>C	NP_002867.1:p.Leu69Pro
NM_058216.2:c.206T>C	NP_478123.1:p.Leu69Pro
NR_103872.1:n.277T>C
NR_103872.2:n.248T>C
NR_103873.1:n.174T>C
ENST00000337432.8:c.206T>C	ENSP00000336701.4:p.Leu69Pro
ENST00000421782.3:c.206T>C	ENSP00000391450.2:p.Leu69Pro
ENST00000425173.5:c.2T>C	ENSP00000407282.1:p.Leu1Pro
ENST00000461271.5:c.-146T>C	ENSP00000464056.1:n.-146T>C
ENST00000461271.6:c.-146T>C	ENSP00000464056.2:n.-146T>C
ENST00000475762.5:c.*909T>C	ENSP00000432421.1:n.*909T>C
ENST00000482007.5:c.206T>C	ENSP00000433332.1:p.Leu69Pro
ENST00000486827.1:c.*1070T>C	ENSP00000436761.1:n.*1070T>C
ENST00000487525.5:c.206T>C	ENSP00000431637.1:p.Leu69Pro
ENST00000487921.5:n.118T>C
ENST00000583539.5:c.206T>C	ENSP00000463121.1:p.Leu69Pro
ENST00000584617.5:c.127-1702T>C
ENST00000697675.1:n.1300T>C
ENST00000697676.1:n.266T>C
ENST00000697677.1:n.1287T>C
ENST00000697678.1:n.108T>C
ENST00000697679.1:n.1280T>C
ENST00000697680.1:c.*1070T>C	ENSP00000513392.1:n.*1070T>C
ENST00000697681.1:c.*1070T>C	ENSP00000513393.1:n.*1070T>C
ENST00000697683.1:c.*1070T>C	ENSP00000513395.1:n.*1070T>C
ENST00000697684.1:n.266T>C
ENST00000697685.1:c.*1070T>C	ENSP00000513396.1:n.*1070T>C
ENST00000697686.1:c.-146T>C	ENSP00000513397.1:n.-146T>C
ENST00000697687.1:n.252T>C
ENST00000697688.1:n.252T>C
ENST00000697689.1:c.*909T>C	ENSP00000513398.1:n.*909T>C
ENST00000697690.1:c.206T>C	ENSP00000513399.1:p.Leu69Pro
ENST00000697691.1:c.*178T>C	ENSP00000513400.1:n.*178T>C
ENST00000697692.1:c.*218T>C	ENSP00000513401.1:n.*218T>C
ENST00000697693.1:n.981T>C
ENST00000697694.1:c.-146T>C	ENSP00000513402.1:n.-146T>C
ENST00000697695.1:n.813T>C
XM_006722001.2:c.206T>C	XP_006722064.1:p.Leu69Pro
XM_006722001.4:c.206T>C	XP_006722064.1:p.Leu69Pro
XM_006722002.2:c.206T>C	XP_006722065.1:p.Leu69Pro
XM_006722002.4:c.206T>C	XP_006722065.1:p.Leu69Pro
XM_006722004.2:c.-146T>C	XP_006722067.1:n.-146T>C
XM_006722004.3:c.-146T>C	XP_006722067.1:n.-146T>C
XM_006722005.2:c.-146T>C	XP_006722068.1:n.-146T>C
XM_006722005.3:c.-146T>C	XP_006722068.1:n.-146T>C
XM_011525092.1:c.-146T>C	XP_011523394.1:n.-146T>C
XM_011525092.2:c.-146T>C	XP_011523394.1:n.-146T>C
XM_011525093.1:c.-146T>C	XP_011523395.1:n.-146T>C
XM_011525093.2:c.-146T>C	XP_011523395.1:n.-146T>C
XM_011525094.1:c.-146T>C	XP_011523396.1:n.-146T>C
XM_011525094.2:c.-146T>C	XP_011523396.1:n.-146T>C
XM_017024914.1:c.-146T>C	XP_016880403.1:n.-146T>C
XM_017024915.1:c.-146T>C	XP_016880404.1:n.-146T>C
XM_017024916.1:c.-146T>C	XP_016880405.1:n.-146T>C
XM_017024917.1:c.-146T>C	XP_016880406.1:n.-146T>C
XM_017024918.2:c.-146T>C	XP_016880407.1:n.-146T>C
XM_017024919.1:c.-146T>C	XP_016880408.1:n.-146T>C
XR_934513.1:n.279T>C
XR_934513.3:n.710T>C
XR_934514.1:n.279T>C
XR_934514.3:n.710T>C