Canonical Allele Identifier: CA2638988693

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58692610-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692610T>C , CM000679.2:g.58692610T>C	GRCh38
NC_000017.10:g.56769971T>C , CM000679.1:g.56769971T>C	GRCh37
NC_000017.9:g.54124970T>C	NCBI36
NG_023199.1:g.5009T>C , LRG_314:g.5009T>C
NG_047169.1:g.4470A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-282T>C	ENSP00000464056.2:n.-282T>C
ENST00000697675.1:n.38T>C
ENST00000697676.1:n.27T>C
ENST00000697677.1:n.25T>C
ENST00000697678.1:n.25T>C
ENST00000697679.1:n.18T>C
ENST00000697680.1:c.-34T>C	ENSP00000513392.1:n.-34T>C
ENST00000697681.1:c.-34T>C	ENSP00000513393.1:n.-34T>C
ENST00000697683.1:c.-34T>C	ENSP00000513395.1:n.-34T>C
ENST00000697684.1:n.27T>C
ENST00000697685.1:c.-34T>C	ENSP00000513396.1:n.-34T>C
ENST00000697686.1:c.-229T>C	ENSP00000513397.1:n.-229T>C
ENST00000697687.1:n.13T>C
ENST00000697688.1:n.13T>C
ENST00000697689.1:c.-34T>C	ENSP00000513398.1:n.-34T>C
ENST00000697690.1:c.-34T>C	ENSP00000513399.1:n.-34T>C
ENST00000337432.9:c.-34T>C MANE Select	ENSP00000336701.4:n.-34T>C
ENST00000337432.8:c.-34T>C	ENSP00000336701.4:n.-34T>C
ENST00000461271.5:c.-282T>C	ENSP00000464056.1:n.-282T>C
ENST00000475762.5:c.-34T>C	ENSP00000432421.1:n.-34T>C
ENST00000476741.2:n.9T>C
ENST00000486827.1:c.-34T>C	ENSP00000436761.1:n.-34T>C
ENST00000487525.5:c.-34T>C	ENSP00000431637.1:n.-34T>C
ENST00000487921.5:n.35T>C
ENST00000583539.5:c.-34T>C	ENSP00000463121.1:n.-34T>C
NM_002876.3:c.-34T>C	NP_002867.1:n.-34T>C
NM_058216.2:c.-34T>C	NP_478123.1:n.-34T>C
NR_103872.1:n.38T>C
NR_103873.1:n.38T>C
XM_006722001.2:c.-34T>C	XP_006722064.1:n.-34T>C
XM_006722002.2:c.-34T>C	XP_006722065.1:n.-34T>C
XM_006722004.2:c.-282T>C	XP_006722067.1:n.-282T>C
XM_006722005.2:c.-229T>C	XP_006722068.1:n.-229T>C
XM_011525092.1:c.-582T>C	XP_011523394.1:n.-582T>C
XM_011525093.1:c.-743T>C	XP_011523395.1:n.-743T>C
XR_934513.1:n.40T>C
XR_934514.1:n.40T>C
XM_006722001.4:c.-34T>C	XP_006722064.1:n.-34T>C
XM_006722002.4:c.-34T>C	XP_006722065.1:n.-34T>C
XM_006722004.3:c.-282T>C	XP_006722067.1:n.-282T>C
XM_006722005.3:c.-229T>C	XP_006722068.1:n.-229T>C
XM_017024914.1:c.-282T>C	XP_016880403.1:n.-282T>C
XM_017024917.1:c.-229T>C	XP_016880406.1:n.-229T>C
XR_934513.3:n.471T>C
XR_934514.3:n.471T>C
NM_058216.3:c.-34T>C MANE Select	NP_478123.1:n.-34T>C
NR_103872.2:n.9T>C
NM_002876.4:c.-34T>C	NP_002867.1:n.-34T>C