Canonical Allele Identifier: CA400339888

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 538773
• ClinVar RCV Id: RCV000648238
• dbSNP Id: rs1555593511
• gnomAD v4: 17-58694976-T-C
• MyVariant Identifiers: chr17:g.56772337T>C (hg19) ; chr17:g.58694976T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694976T>C , CM000679.2:g.58694976T>C	GRCh38
NC_000017.10:g.56772337T>C , CM000679.1:g.56772337T>C	GRCh37
NC_000017.9:g.54127336T>C	NCBI36
NG_023199.1:g.7375T>C , LRG_314:g.7375T>C
NG_047169.1:g.2104A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-161T>C	ENSP00000464056.2:n.-161T>C
ENST00000697675.1:n.1285T>C
ENST00000697676.1:n.251T>C
ENST00000697677.1:n.1272T>C
ENST00000697678.1:n.93T>C
ENST00000697679.1:n.1265T>C
ENST00000697680.1:c.*1055T>C	ENSP00000513392.1:n.*1055T>C
ENST00000697681.1:c.*1055T>C	ENSP00000513393.1:n.*1055T>C
ENST00000697683.1:c.*1055T>C	ENSP00000513395.1:n.*1055T>C
ENST00000697684.1:n.251T>C
ENST00000697685.1:c.*1055T>C	ENSP00000513396.1:n.*1055T>C
ENST00000697686.1:c.-161T>C	ENSP00000513397.1:n.-161T>C
ENST00000697687.1:n.237T>C
ENST00000697688.1:n.237T>C
ENST00000697689.1:c.*894T>C	ENSP00000513398.1:n.*894T>C
ENST00000697690.1:c.191T>C	ENSP00000513399.1:p.Ile64Thr
ENST00000697691.1:c.*163T>C	ENSP00000513400.1:n.*163T>C
ENST00000697692.1:c.*203T>C	ENSP00000513401.1:n.*203T>C
ENST00000697693.1:n.966T>C
ENST00000697694.1:c.-161T>C	ENSP00000513402.1:n.-161T>C
ENST00000697695.1:n.798T>C
ENST00000337432.9:c.191T>C MANE Select	ENSP00000336701.4:p.Ile64Thr
ENST00000337432.8:c.191T>C	ENSP00000336701.4:p.Ile64Thr
ENST00000421782.3:c.191T>C	ENSP00000391450.2:p.Ile64Thr
ENST00000461271.5:c.-161T>C	ENSP00000464056.1:n.-161T>C
ENST00000475762.5:c.*894T>C	ENSP00000432421.1:n.*894T>C
ENST00000482007.5:c.191T>C	ENSP00000433332.1:p.Ile64Thr
ENST00000486827.1:c.*1055T>C	ENSP00000436761.1:n.*1055T>C
ENST00000487525.5:c.191T>C	ENSP00000431637.1:p.Ile64Thr
ENST00000487921.5:n.103T>C
ENST00000583539.5:c.191T>C	ENSP00000463121.1:p.Ile64Thr
ENST00000584617.5:c.127-1717T>C
NM_002876.3:c.191T>C	NP_002867.1:p.Ile64Thr
NM_058216.2:c.191T>C	NP_478123.1:p.Ile64Thr
NR_103872.1:n.262T>C
NR_103873.1:n.159T>C
XM_006722001.2:c.191T>C	XP_006722064.1:p.Ile64Thr
XM_006722002.2:c.191T>C	XP_006722065.1:p.Ile64Thr
XM_006722004.2:c.-161T>C	XP_006722067.1:n.-161T>C
XM_006722005.2:c.-161T>C	XP_006722068.1:n.-161T>C
XM_011525092.1:c.-161T>C	XP_011523394.1:n.-161T>C
XM_011525093.1:c.-161T>C	XP_011523395.1:n.-161T>C
XM_011525094.1:c.-161T>C	XP_011523396.1:n.-161T>C
XR_934513.1:n.264T>C
XR_934514.1:n.264T>C
XM_006722001.4:c.191T>C	XP_006722064.1:p.Ile64Thr
XM_006722002.4:c.191T>C	XP_006722065.1:p.Ile64Thr
XM_006722004.3:c.-161T>C	XP_006722067.1:n.-161T>C
XM_006722005.3:c.-161T>C	XP_006722068.1:n.-161T>C
XM_011525092.2:c.-161T>C	XP_011523394.1:n.-161T>C
XM_011525093.2:c.-161T>C	XP_011523395.1:n.-161T>C
XM_011525094.2:c.-161T>C	XP_011523396.1:n.-161T>C
XM_017024914.1:c.-161T>C	XP_016880403.1:n.-161T>C
XM_017024915.1:c.-161T>C	XP_016880404.1:n.-161T>C
XM_017024916.1:c.-161T>C	XP_016880405.1:n.-161T>C
XM_017024917.1:c.-161T>C	XP_016880406.1:n.-161T>C
XM_017024918.2:c.-161T>C	XP_016880407.1:n.-161T>C
XM_017024919.1:c.-161T>C	XP_016880408.1:n.-161T>C
XR_934513.3:n.695T>C
XR_934514.3:n.695T>C
NM_058216.3:c.191T>C MANE Select	NP_478123.1:p.Ile64Thr
NR_103872.2:n.233T>C
NM_002876.4:c.191T>C	NP_002867.1:p.Ile64Thr