Canonical Allele Identifier: CA400343746

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56774062T>A (hg19) ; chr17:g.58696701T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696701T>A , CM000679.2:g.58696701T>A	GRCh38
NC_000017.10:g.56774062T>A , CM000679.1:g.56774062T>A	GRCh37
NC_000017.9:g.54129061T>A	NCBI36
NG_023199.1:g.9100T>A , LRG_314:g.9100T>A
NG_047169.1:g.379A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.62T>A	ENSP00000464056.2:p.Leu21Ter
ENST00000697675.1:n.3010T>A
ENST00000697676.1:n.473T>A
ENST00000697677.1:n.1494T>A
ENST00000697678.1:n.315T>A
ENST00000697679.1:n.1487T>A
ENST00000697680.1:c.*1277T>A	ENSP00000513392.1:n.*1277T>A
ENST00000697681.1:c.*1304T>A	ENSP00000513393.1:n.*1304T>A
ENST00000697683.1:c.*1277T>A	ENSP00000513395.1:n.*1277T>A
ENST00000697684.1:n.473T>A
ENST00000697685.1:c.*1268+1512T>A	ENSP00000513396.1:n.*1268+1512T>A
ENST00000697686.1:c.62T>A	ENSP00000513397.1:p.Leu21Ter
ENST00000697687.1:n.450+1512T>A
ENST00000697688.1:n.459T>A
ENST00000697689.1:c.*1107+1512T>A	ENSP00000513398.1:n.*1107+1512T>A
ENST00000697690.1:c.413T>A	ENSP00000513399.1:p.Leu138Ter
ENST00000697691.1:c.*385T>A	ENSP00000513400.1:n.*385T>A
ENST00000697692.1:c.*425T>A	ENSP00000513401.1:n.*425T>A
ENST00000697694.1:c.62T>A	ENSP00000513402.1:p.Leu21Ter
ENST00000697695.1:n.1020T>A
ENST00000337432.9:c.413T>A MANE Select	ENSP00000336701.4:p.Leu138Ter
ENST00000337432.8:c.413T>A	ENSP00000336701.4:p.Leu138Ter
ENST00000413590.5:c.51T>A
ENST00000425173.5:c.209T>A	ENSP00000407282.1:p.Leu70Ter
ENST00000461271.5:c.62T>A	ENSP00000464056.1:p.Leu21Ter
ENST00000475762.5:c.*1116T>A	ENSP00000432421.1:n.*1116T>A
ENST00000482007.5:c.404+1512T>A	ENSP00000433332.1:n.404+1512T>A
ENST00000487525.5:c.404+1512T>A	ENSP00000431637.1:n.404+1512T>A
ENST00000487921.5:n.325T>A
ENST00000583539.5:c.413T>A	ENSP00000463121.1:p.Leu138Ter
ENST00000584617.5:c.135T>A
ENST00000622327.4:c.149T>A	ENSP00000482326.1:p.Leu50Ter
NM_058216.2:c.413T>A	NP_478123.1:p.Leu138Ter
NR_103872.1:n.475+1512T>A
XM_006722001.2:c.413T>A	XP_006722064.1:p.Leu138Ter
XM_006722002.2:c.413T>A	XP_006722065.1:p.Leu138Ter
XM_006722004.2:c.62T>A	XP_006722067.1:p.Leu21Ter
XM_006722005.2:c.62T>A	XP_006722068.1:p.Leu21Ter
XM_011525092.1:c.62T>A	XP_011523394.1:p.Leu21Ter
XM_011525093.1:c.62T>A	XP_011523395.1:p.Leu21Ter
XM_011525094.1:c.62T>A	XP_011523396.1:p.Leu21Ter
XR_934513.1:n.486T>A
XR_934514.1:n.486T>A
XM_006722001.4:c.413T>A	XP_006722064.1:p.Leu138Ter
XM_006722002.4:c.413T>A	XP_006722065.1:p.Leu138Ter
XM_006722004.3:c.62T>A	XP_006722067.1:p.Leu21Ter
XM_006722005.3:c.62T>A	XP_006722068.1:p.Leu21Ter
XM_011525092.2:c.62T>A	XP_011523394.1:p.Leu21Ter
XM_011525093.2:c.62T>A	XP_011523395.1:p.Leu21Ter
XM_011525094.2:c.62T>A	XP_011523396.1:p.Leu21Ter
XM_017024914.1:c.62T>A	XP_016880403.1:p.Leu21Ter
XM_017024915.1:c.62T>A	XP_016880404.1:p.Leu21Ter
XM_017024916.1:c.62T>A	XP_016880405.1:p.Leu21Ter
XM_017024917.1:c.62T>A	XP_016880406.1:p.Leu21Ter
XM_017024918.2:c.62T>A	XP_016880407.1:p.Leu21Ter
XM_017024919.1:c.62T>A	XP_016880408.1:p.Leu21Ter
XR_934513.3:n.917T>A
XR_934514.3:n.917T>A
NM_058216.3:c.413T>A MANE Select	NP_478123.1:p.Leu138Ter
NR_103872.2:n.446+1512T>A