Canonical Allele Identifier: CA400341934

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56772531G>C (hg19) ; chr17:g.58695170G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695170G>C , CM000679.2:g.58695170G>C	GRCh38
NC_000017.10:g.56772531G>C , CM000679.1:g.56772531G>C	GRCh37
NC_000017.9:g.54127530G>C	NCBI36
NG_023199.1:g.7569G>C , LRG_314:g.7569G>C
NG_047169.1:g.1910C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.34G>C	ENSP00000464056.2:p.Val12Leu
ENST00000697675.1:n.1479G>C
ENST00000697676.1:n.445G>C
ENST00000697677.1:n.1466G>C
ENST00000697678.1:n.287G>C
ENST00000697679.1:n.1459G>C
ENST00000697680.1:c.*1249G>C	ENSP00000513392.1:n.*1249G>C
ENST00000697681.1:c.*1249G>C	ENSP00000513393.1:n.*1249G>C
ENST00000697683.1:c.*1249G>C	ENSP00000513395.1:n.*1249G>C
ENST00000697684.1:n.445G>C
ENST00000697685.1:c.*1249G>C	ENSP00000513396.1:n.*1249G>C
ENST00000697686.1:c.34G>C	ENSP00000513397.1:p.Val12Leu
ENST00000697687.1:n.431G>C
ENST00000697688.1:n.431G>C
ENST00000697689.1:c.*1088G>C	ENSP00000513398.1:n.*1088G>C
ENST00000697690.1:c.385G>C	ENSP00000513399.1:p.Val129Leu
ENST00000697691.1:c.*357G>C	ENSP00000513400.1:n.*357G>C
ENST00000697692.1:c.*397G>C	ENSP00000513401.1:n.*397G>C
ENST00000697693.1:n.1160G>C
ENST00000697694.1:c.34G>C	ENSP00000513402.1:p.Val12Leu
ENST00000697695.1:n.992G>C
ENST00000337432.9:c.385G>C MANE Select	ENSP00000336701.4:p.Val129Leu
ENST00000337432.8:c.385G>C	ENSP00000336701.4:p.Val129Leu
ENST00000413590.5:c.23G>C
ENST00000421782.3:c.385G>C	ENSP00000391450.2:p.Val129Leu
ENST00000425173.5:c.181G>C	ENSP00000407282.1:p.Val61Leu
ENST00000461271.5:c.34G>C	ENSP00000464056.1:p.Val12Leu
ENST00000475762.5:c.*1088G>C	ENSP00000432421.1:n.*1088G>C
ENST00000482007.5:c.385G>C	ENSP00000433332.1:p.Val129Leu
ENST00000486827.1:c.*1249G>C	ENSP00000436761.1:n.*1249G>C
ENST00000487525.5:c.385G>C	ENSP00000431637.1:p.Val129Leu
ENST00000487921.5:n.297G>C
ENST00000583539.5:c.385G>C	ENSP00000463121.1:p.Val129Leu
ENST00000584617.5:c.127-1523G>C
ENST00000622327.4:c.121G>C	ENSP00000482326.1:p.Val41Leu
NM_002876.3:c.385G>C	NP_002867.1:p.Val129Leu
NM_058216.2:c.385G>C	NP_478123.1:p.Val129Leu
NR_103872.1:n.456G>C
NR_103873.1:n.353G>C
XM_006722001.2:c.385G>C	XP_006722064.1:p.Val129Leu
XM_006722002.2:c.385G>C	XP_006722065.1:p.Val129Leu
XM_006722004.2:c.34G>C	XP_006722067.1:p.Val12Leu
XM_006722005.2:c.34G>C	XP_006722068.1:p.Val12Leu
XM_011525092.1:c.34G>C	XP_011523394.1:p.Val12Leu
XM_011525093.1:c.34G>C	XP_011523395.1:p.Val12Leu
XM_011525094.1:c.34G>C	XP_011523396.1:p.Val12Leu
XR_934513.1:n.458G>C
XR_934514.1:n.458G>C
XM_006722001.4:c.385G>C	XP_006722064.1:p.Val129Leu
XM_006722002.4:c.385G>C	XP_006722065.1:p.Val129Leu
XM_006722004.3:c.34G>C	XP_006722067.1:p.Val12Leu
XM_006722005.3:c.34G>C	XP_006722068.1:p.Val12Leu
XM_011525092.2:c.34G>C	XP_011523394.1:p.Val12Leu
XM_011525093.2:c.34G>C	XP_011523395.1:p.Val12Leu
XM_011525094.2:c.34G>C	XP_011523396.1:p.Val12Leu
XM_017024914.1:c.34G>C	XP_016880403.1:p.Val12Leu
XM_017024915.1:c.34G>C	XP_016880404.1:p.Val12Leu
XM_017024916.1:c.34G>C	XP_016880405.1:p.Val12Leu
XM_017024917.1:c.34G>C	XP_016880406.1:p.Val12Leu
XM_017024918.2:c.34G>C	XP_016880407.1:p.Val12Leu
XM_017024919.1:c.34G>C	XP_016880408.1:p.Val12Leu
XR_934513.3:n.889G>C
XR_934514.3:n.889G>C
NM_058216.3:c.385G>C MANE Select	NP_478123.1:p.Val129Leu
NR_103872.2:n.427G>C
NM_002876.4:c.385G>C	NP_002867.1:p.Val129Leu