Canonical Allele Identifier: CA2638988638

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143667055
• gnomAD v4: 17-58692581-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692581G>C , CM000679.2:g.58692581G>C	GRCh38
NC_000017.10:g.56769942G>C , CM000679.1:g.56769942G>C	GRCh37
NC_000017.9:g.54124941G>C	NCBI36
NG_023199.1:g.4980G>C , LRG_314:g.4980G>C
NG_047169.1:g.4499C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-311G>C	ENSP00000464056.2:n.-311G>C
ENST00000697675.1:n.9G>C
ENST00000697683.1:c.-63G>C	ENSP00000513395.1:n.-63G>C
ENST00000337432.8:c.-63G>C	ENSP00000336701.4:n.-63G>C
ENST00000461271.5:c.-311G>C	ENSP00000464056.1:n.-311G>C
ENST00000487921.5:n.6G>C
ENST00000583539.5:c.-63G>C	ENSP00000463121.1:n.-63G>C
NM_002876.3:c.-63G>C	NP_002867.1:n.-63G>C
NM_058216.2:c.-63G>C	NP_478123.1:n.-63G>C
NR_103872.1:n.9G>C
NR_103873.1:n.9G>C
XM_006722001.2:c.-63G>C	XP_006722064.1:n.-63G>C
XM_006722002.2:c.-63G>C	XP_006722065.1:n.-63G>C
XM_006722004.2:c.-311G>C	XP_006722067.1:n.-311G>C
XM_006722005.2:c.-258G>C	XP_006722068.1:n.-258G>C
XR_934513.1:n.11G>C
XR_934514.1:n.11G>C
XM_006722001.4:c.-63G>C	XP_006722064.1:n.-63G>C
XM_006722002.4:c.-63G>C	XP_006722065.1:n.-63G>C
XM_006722004.3:c.-311G>C	XP_006722067.1:n.-311G>C
XM_006722005.3:c.-258G>C	XP_006722068.1:n.-258G>C
XM_017024914.1:c.-311G>C	XP_016880403.1:n.-311G>C
XM_017024917.1:c.-258G>C	XP_016880406.1:n.-258G>C
XR_934513.3:n.442G>C
XR_934514.3:n.442G>C