Canonical Allele Identifier: CA8677294

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 630133
• ClinVar RCV Id: RCV000775206 ; RCV001201900
• dbSNP Id: rs748043225
• ExAC: 17:56780689 A / C
• gnomAD v2: 17-56780689-A-C
• gnomAD v4: 17-58703328-A-C
• MyVariant Identifiers: chr17:g.56780689A>C (hg19) ; chr17:g.58703328A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703328A>C , CM000679.2:g.58703328A>C	GRCh38
NC_000017.10:g.56780689A>C , CM000679.1:g.56780689A>C	GRCh37
NC_000017.9:g.54135688A>C	NCBI36
NG_023199.1:g.15727A>C , LRG_314:g.15727A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.353A>C	ENSP00000464056.2:p.Lys118Thr
ENST00000697677.1:n.1785A>C
ENST00000697678.1:n.606A>C
ENST00000697679.1:n.1778A>C
ENST00000697680.1:c.*1568A>C	ENSP00000513392.1:n.*1568A>C
ENST00000697681.1:c.*1720A>C	ENSP00000513393.1:n.*1720A>C
ENST00000697683.1:c.*1568A>C	ENSP00000513395.1:n.*1568A>C
ENST00000697684.1:n.764A>C
ENST00000697685.1:c.*1401A>C	ENSP00000513396.1:n.*1401A>C
ENST00000697686.1:c.353A>C	ENSP00000513397.1:p.Lys118Thr
ENST00000697687.1:n.583A>C
ENST00000697688.1:n.750A>C
ENST00000697689.1:c.*1240A>C	ENSP00000513398.1:n.*1240A>C
ENST00000697690.1:c.704A>C	ENSP00000513399.1:p.Lys235Thr
ENST00000697691.1:c.*676A>C	ENSP00000513400.1:n.*676A>C
ENST00000697692.1:c.*716A>C	ENSP00000513401.1:n.*716A>C
ENST00000697694.1:c.353A>C	ENSP00000513402.1:p.Lys118Thr
ENST00000697695.1:n.1311A>C
ENST00000337432.9:c.704A>C MANE Select	ENSP00000336701.4:p.Lys235Thr
ENST00000337432.8:c.704A>C	ENSP00000336701.4:p.Lys235Thr
ENST00000413590.5:c.342A>C
ENST00000425173.5:c.500A>C	ENSP00000407282.1:p.Lys167Thr
ENST00000461271.5:c.353A>C	ENSP00000464056.1:p.Lys118Thr
ENST00000475762.5:c.*1407A>C	ENSP00000432421.1:n.*1407A>C
ENST00000482007.5:c.*132A>C	ENSP00000433332.1:n.*132A>C
ENST00000487525.5:c.*132A>C	ENSP00000431637.1:n.*132A>C
ENST00000487921.5:n.616A>C
ENST00000583539.5:c.704A>C	ENSP00000463121.1:p.Lys235Thr
ENST00000584617.5:c.426A>C
NM_058216.2:c.704A>C	NP_478123.1:p.Lys235Thr
NR_103872.1:n.608A>C
XM_006722001.2:c.704A>C	XP_006722064.1:p.Lys235Thr
XM_006722002.2:c.704A>C	XP_006722065.1:p.Lys235Thr
XM_006722004.2:c.353A>C	XP_006722067.1:p.Lys118Thr
XM_006722005.2:c.353A>C	XP_006722068.1:p.Lys118Thr
XM_011525092.1:c.353A>C	XP_011523394.1:p.Lys118Thr
XM_011525093.1:c.353A>C	XP_011523395.1:p.Lys118Thr
XM_011525094.1:c.353A>C	XP_011523396.1:p.Lys118Thr
XR_934513.1:n.777A>C
XR_934514.1:n.777A>C
XM_006722001.4:c.704A>C	XP_006722064.1:p.Lys235Thr
XM_006722002.4:c.704A>C	XP_006722065.1:p.Lys235Thr
XM_006722004.3:c.353A>C	XP_006722067.1:p.Lys118Thr
XM_006722005.3:c.353A>C	XP_006722068.1:p.Lys118Thr
XM_011525092.2:c.353A>C	XP_011523394.1:p.Lys118Thr
XM_011525093.2:c.353A>C	XP_011523395.1:p.Lys118Thr
XM_011525094.2:c.353A>C	XP_011523396.1:p.Lys118Thr
XM_017024914.1:c.353A>C	XP_016880403.1:p.Lys118Thr
XM_017024915.1:c.353A>C	XP_016880404.1:p.Lys118Thr
XM_017024916.1:c.353A>C	XP_016880405.1:p.Lys118Thr
XM_017024917.1:c.353A>C	XP_016880406.1:p.Lys118Thr
XM_017024918.2:c.353A>C	XP_016880407.1:p.Lys118Thr
XM_017024919.1:c.353A>C	XP_016880408.1:p.Lys118Thr
XR_934513.3:n.1208A>C
XR_934514.3:n.1208A>C
NM_058216.3:c.704A>C MANE Select	NP_478123.1:p.Lys235Thr
NR_103872.2:n.579A>C