Canonical Allele Identifier: CA400349992

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143801157
• gnomAD v4: 17-58703306-G-C
• MyVariant Identifiers: chr17:g.56780667G>C (hg19) ; chr17:g.58703306G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703306G>C , CM000679.2:g.58703306G>C	GRCh38
NC_000017.10:g.56780667G>C , CM000679.1:g.56780667G>C	GRCh37
NC_000017.9:g.54135666G>C	NCBI36
NG_023199.1:g.15705G>C , LRG_314:g.15705G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.331G>C	ENSP00000464056.2:p.Asp111His
ENST00000697677.1:n.1763G>C
ENST00000697678.1:n.584G>C
ENST00000697679.1:n.1756G>C
ENST00000697680.1:c.*1546G>C	ENSP00000513392.1:n.*1546G>C
ENST00000697681.1:c.*1698G>C	ENSP00000513393.1:n.*1698G>C
ENST00000697683.1:c.*1546G>C	ENSP00000513395.1:n.*1546G>C
ENST00000697684.1:n.742G>C
ENST00000697685.1:c.*1379G>C	ENSP00000513396.1:n.*1379G>C
ENST00000697686.1:c.331G>C	ENSP00000513397.1:p.Asp111His
ENST00000697687.1:n.561G>C
ENST00000697688.1:n.728G>C
ENST00000697689.1:c.*1218G>C	ENSP00000513398.1:n.*1218G>C
ENST00000697690.1:c.682G>C	ENSP00000513399.1:p.Asp228His
ENST00000697691.1:c.*654G>C	ENSP00000513400.1:n.*654G>C
ENST00000697692.1:c.*694G>C	ENSP00000513401.1:n.*694G>C
ENST00000697694.1:c.331G>C	ENSP00000513402.1:p.Asp111His
ENST00000697695.1:n.1289G>C
ENST00000337432.9:c.682G>C MANE Select	ENSP00000336701.4:p.Asp228His
ENST00000337432.8:c.682G>C	ENSP00000336701.4:p.Asp228His
ENST00000413590.5:c.320G>C
ENST00000425173.5:c.478G>C	ENSP00000407282.1:p.Asp160His
ENST00000461271.5:c.331G>C	ENSP00000464056.1:p.Asp111His
ENST00000475762.5:c.*1385G>C	ENSP00000432421.1:n.*1385G>C
ENST00000482007.5:c.*110G>C	ENSP00000433332.1:n.*110G>C
ENST00000487525.5:c.*110G>C	ENSP00000431637.1:n.*110G>C
ENST00000487921.5:n.594G>C
ENST00000583539.5:c.682G>C	ENSP00000463121.1:p.Asp228His
ENST00000584617.5:c.404G>C
NM_058216.2:c.682G>C	NP_478123.1:p.Asp228His
NR_103872.1:n.586G>C
XM_006722001.2:c.682G>C	XP_006722064.1:p.Asp228His
XM_006722002.2:c.682G>C	XP_006722065.1:p.Asp228His
XM_006722004.2:c.331G>C	XP_006722067.1:p.Asp111His
XM_006722005.2:c.331G>C	XP_006722068.1:p.Asp111His
XM_011525092.1:c.331G>C	XP_011523394.1:p.Asp111His
XM_011525093.1:c.331G>C	XP_011523395.1:p.Asp111His
XM_011525094.1:c.331G>C	XP_011523396.1:p.Asp111His
XR_934513.1:n.755G>C
XR_934514.1:n.755G>C
XM_006722001.4:c.682G>C	XP_006722064.1:p.Asp228His
XM_006722002.4:c.682G>C	XP_006722065.1:p.Asp228His
XM_006722004.3:c.331G>C	XP_006722067.1:p.Asp111His
XM_006722005.3:c.331G>C	XP_006722068.1:p.Asp111His
XM_011525092.2:c.331G>C	XP_011523394.1:p.Asp111His
XM_011525093.2:c.331G>C	XP_011523395.1:p.Asp111His
XM_011525094.2:c.331G>C	XP_011523396.1:p.Asp111His
XM_017024914.1:c.331G>C	XP_016880403.1:p.Asp111His
XM_017024915.1:c.331G>C	XP_016880404.1:p.Asp111His
XM_017024916.1:c.331G>C	XP_016880405.1:p.Asp111His
XM_017024917.1:c.331G>C	XP_016880406.1:p.Asp111His
XM_017024918.2:c.331G>C	XP_016880407.1:p.Asp111His
XM_017024919.1:c.331G>C	XP_016880408.1:p.Asp111His
XR_934513.3:n.1186G>C
XR_934514.3:n.1186G>C
NM_058216.3:c.682G>C MANE Select	NP_478123.1:p.Asp228His
NR_103872.2:n.557G>C