Canonical Allele Identifier: CA2267815256

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695015G= , CM000679.2:g.58695015G=	GRCh38
NC_000017.10:g.56772376G= , CM000679.1:g.56772376G=	GRCh37
NC_000017.9:g.54127375G=	NCBI36
NG_023199.1:g.7414G= , LRG_314:g.7414G=
NG_047169.1:g.2065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-122G=	ENSP00000464056.2:n.-122G=
ENST00000697675.1:n.1324G=
ENST00000697676.1:n.290G=
ENST00000697677.1:n.1311G=
ENST00000697678.1:n.132G=
ENST00000697679.1:n.1304G=
ENST00000697680.1:c.*1094G=	ENSP00000513392.1:n.*1094G=
ENST00000697681.1:c.*1094G=	ENSP00000513393.1:n.*1094G=
ENST00000697683.1:c.*1094G=	ENSP00000513395.1:n.*1094G=
ENST00000697684.1:n.290G=
ENST00000697685.1:c.*1094G=	ENSP00000513396.1:n.*1094G=
ENST00000697686.1:c.-122G=	ENSP00000513397.1:n.-122G=
ENST00000697687.1:n.276G=
ENST00000697688.1:n.276G=
ENST00000697689.1:c.*933G=	ENSP00000513398.1:n.*933G=
ENST00000697690.1:c.230G=	ENSP00000513399.1:p.Gly77=
ENST00000697691.1:c.*202G=	ENSP00000513400.1:n.*202G=
ENST00000697692.1:c.*242G=	ENSP00000513401.1:n.*242G=
ENST00000697693.1:n.1005G=
ENST00000697694.1:c.-122G=	ENSP00000513402.1:n.-122G=
ENST00000697695.1:n.837G=
ENST00000337432.9:c.230G= MANE Select	ENSP00000336701.4:p.Gly77=
ENST00000337432.8:c.230G=	ENSP00000336701.4:p.Gly77=
ENST00000421782.3:c.230G=	ENSP00000391450.2:p.Gly77=
ENST00000425173.5:c.26G=	ENSP00000407282.1:p.Gly9=
ENST00000461271.5:c.-122G=	ENSP00000464056.1:n.-122G=
ENST00000475762.5:c.*933G=	ENSP00000432421.1:n.*933G=
ENST00000482007.5:c.230G=	ENSP00000433332.1:p.Gly77=
ENST00000486827.1:c.*1094G=	ENSP00000436761.1:n.*1094G=
ENST00000487525.5:c.230G=	ENSP00000431637.1:p.Gly77=
ENST00000487921.5:n.142G=
ENST00000583539.5:c.230G=	ENSP00000463121.1:p.Gly77=
ENST00000584617.5:c.127-1678G=
NM_002876.3:c.230G=	NP_002867.1:p.Gly77=
NM_058216.2:c.230G=	NP_478123.1:p.Gly77=
NR_103872.1:n.301G=
NR_103873.1:n.198G=
XM_006722001.2:c.230G=	XP_006722064.1:p.Gly77=
XM_006722002.2:c.230G=	XP_006722065.1:p.Gly77=
XM_006722004.2:c.-122G=	XP_006722067.1:n.-122G=
XM_006722005.2:c.-122G=	XP_006722068.1:n.-122G=
XM_011525092.1:c.-122G=	XP_011523394.1:n.-122G=
XM_011525093.1:c.-122G=	XP_011523395.1:n.-122G=
XM_011525094.1:c.-122G=	XP_011523396.1:n.-122G=
XR_934513.1:n.303G=
XR_934514.1:n.303G=
XM_006722001.4:c.230G=	XP_006722064.1:p.Gly77=
XM_006722002.4:c.230G=	XP_006722065.1:p.Gly77=
XM_006722004.3:c.-122G=	XP_006722067.1:n.-122G=
XM_006722005.3:c.-122G=	XP_006722068.1:n.-122G=
XM_011525092.2:c.-122G=	XP_011523394.1:n.-122G=
XM_011525093.2:c.-122G=	XP_011523395.1:n.-122G=
XM_011525094.2:c.-122G=	XP_011523396.1:n.-122G=
XM_017024914.1:c.-122G=	XP_016880403.1:n.-122G=
XM_017024915.1:c.-122G=	XP_016880404.1:n.-122G=
XM_017024916.1:c.-122G=	XP_016880405.1:n.-122G=
XM_017024917.1:c.-122G=	XP_016880406.1:n.-122G=
XM_017024918.2:c.-122G=	XP_016880407.1:n.-122G=
XM_017024919.1:c.-122G=	XP_016880408.1:n.-122G=
XR_934513.3:n.734G=
XR_934514.3:n.734G=
NM_058216.3:c.230G= MANE Select	NP_478123.1:p.Gly77=
NR_103872.2:n.272G=
NM_002876.4:c.230G=	NP_002867.1:p.Gly77=