Canonical Allele Identifier: CA16615467

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 409866
• ClinVar RCV Id: RCV000473460 ; RCV001026086
• dbSNP Id: rs1060502606
• gnomAD v4: 17-58709866-T-G
• MyVariant Identifiers: chr17:g.56787227T>G (hg19) ; chr17:g.58709866T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709866T>G , CM000679.2:g.58709866T>G	GRCh38
NC_000017.10:g.56787227T>G , CM000679.1:g.56787227T>G	GRCh37
NC_000017.9:g.54142226T>G	NCBI36
NG_023199.1:g.22265T>G , LRG_314:g.22265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.362T>G	ENSP00000464056.2:p.Leu121Arg
ENST00000697678.1:n.615T>G
ENST00000697679.1:n.1787T>G
ENST00000697680.1:c.*1577T>G	ENSP00000513392.1:n.*1577T>G
ENST00000697681.1:c.*1874T>G	ENSP00000513393.1:n.*1874T>G
ENST00000697683.1:c.*1577T>G	ENSP00000513395.1:n.*1577T>G
ENST00000697684.1:n.773T>G
ENST00000697685.1:c.*1410T>G	ENSP00000513396.1:n.*1410T>G
ENST00000697686.1:c.362T>G	ENSP00000513397.1:p.Leu121Arg
ENST00000697687.1:n.592T>G
ENST00000697688.1:n.759T>G
ENST00000697689.1:c.*1249T>G	ENSP00000513398.1:n.*1249T>G
ENST00000697690.1:c.713T>G	ENSP00000513399.1:p.Leu238Arg
ENST00000697691.1:c.*685T>G	ENSP00000513400.1:n.*685T>G
ENST00000697692.1:c.*725T>G	ENSP00000513401.1:n.*725T>G
ENST00000697694.1:c.362T>G	ENSP00000513402.1:p.Leu121Arg
ENST00000697695.1:n.1320T>G
ENST00000337432.9:c.713T>G MANE Select	ENSP00000336701.4:p.Leu238Arg
ENST00000337432.8:c.713T>G	ENSP00000336701.4:p.Leu238Arg
ENST00000413590.5:c.351T>G
ENST00000425173.5:c.629T>G	ENSP00000407282.1:p.Leu210Arg
ENST00000461271.5:c.362T>G	ENSP00000464056.1:p.Leu121Arg
ENST00000475762.5:c.*1416T>G	ENSP00000432421.1:n.*1416T>G
ENST00000482007.5:c.*141T>G	ENSP00000433332.1:n.*141T>G
ENST00000487525.5:c.*286T>G	ENSP00000431637.1:n.*286T>G
ENST00000578151.1:n.48T>G
ENST00000581221.5:n.228T>G
ENST00000583539.5:c.713T>G	ENSP00000463121.1:p.Leu238Arg
ENST00000584617.5:c.435T>G
ENST00000584804.1:c.8T>G	ENSP00000463658.1:p.Leu3Arg
NM_058216.2:c.713T>G	NP_478123.1:p.Leu238Arg
NR_103872.1:n.617T>G
XM_006722001.2:c.713T>G	XP_006722064.1:p.Leu238Arg
XM_006722002.2:c.713T>G	XP_006722065.1:p.Leu238Arg
XM_006722004.2:c.362T>G	XP_006722067.1:p.Leu121Arg
XM_006722005.2:c.362T>G	XP_006722068.1:p.Leu121Arg
XM_011525092.1:c.362T>G	XP_011523394.1:p.Leu121Arg
XM_011525093.1:c.362T>G	XP_011523395.1:p.Leu121Arg
XM_011525094.1:c.362T>G	XP_011523396.1:p.Leu121Arg
XR_934513.1:n.931T>G
XR_934514.1:n.931T>G
XM_006722001.4:c.713T>G	XP_006722064.1:p.Leu238Arg
XM_006722002.4:c.713T>G	XP_006722065.1:p.Leu238Arg
XM_006722004.3:c.362T>G	XP_006722067.1:p.Leu121Arg
XM_006722005.3:c.362T>G	XP_006722068.1:p.Leu121Arg
XM_011525092.2:c.362T>G	XP_011523394.1:p.Leu121Arg
XM_011525093.2:c.362T>G	XP_011523395.1:p.Leu121Arg
XM_011525094.2:c.362T>G	XP_011523396.1:p.Leu121Arg
XM_017024914.1:c.362T>G	XP_016880403.1:p.Leu121Arg
XM_017024915.1:c.362T>G	XP_016880404.1:p.Leu121Arg
XM_017024916.1:c.362T>G	XP_016880405.1:p.Leu121Arg
XM_017024917.1:c.362T>G	XP_016880406.1:p.Leu121Arg
XM_017024918.2:c.362T>G	XP_016880407.1:p.Leu121Arg
XM_017024919.1:c.362T>G	XP_016880408.1:p.Leu121Arg
XR_934513.3:n.1362T>G
XR_934514.3:n.1362T>G
NM_058216.3:c.713T>G MANE Select	NP_478123.1:p.Leu238Arg
NR_103872.2:n.588T>G