Canonical Allele Identifier: CA400365093

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 480498
• ClinVar RCV Id: RCV000567794 ; RCV001354176 ; RCV001764646 ; RCV002291669 ; RCV000648289
• dbSNP Id: rs1057521598
• gnomAD v4: 17-58732526-A-G
• MyVariant Identifiers: chr17:g.56809887A>G (hg19) ; chr17:g.58732526A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732526A>G , CM000679.2:g.58732526A>G	GRCh38
NC_000017.10:g.56809887A>G , CM000679.1:g.56809887A>G	GRCh37
NC_000017.9:g.54164886A>G	NCBI36
NG_023199.1:g.44925A>G , LRG_314:g.44925A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.657A>G	ENSP00000464056.2:p.Thr219=
ENST00000697680.1:c.*1972A>G	ENSP00000513392.1:n.*1972A>G
ENST00000697681.1:c.*2169A>G	ENSP00000513393.1:n.*2169A>G
ENST00000697683.1:c.*1944A>G	ENSP00000513395.1:n.*1944A>G
ENST00000697685.1:c.*1705A>G	ENSP00000513396.1:n.*1705A>G
ENST00000697686.1:c.779A>G	ENSP00000513397.1:p.Gln260Arg
ENST00000697689.1:c.*1441-1592A>G	ENSP00000513398.1:n.*1441-1592A>G
ENST00000697690.1:c.905-1592A>G	ENSP00000513399.1:n.905-1592A>G
ENST00000697691.1:c.*980A>G	ENSP00000513400.1:n.*980A>G
ENST00000697692.1:c.*1020A>G	ENSP00000513401.1:n.*1020A>G
ENST00000697694.1:c.657A>G	ENSP00000513402.1:p.Thr219=
ENST00000697695.1:n.1615A>G
ENST00000337432.9:c.1008A>G MANE Select	ENSP00000336701.4:p.Thr336=
ENST00000337432.8:c.1008A>G	ENSP00000336701.4:p.Thr336=
ENST00000413590.5:c.649A>G
ENST00000461706.1:n.195A>G
ENST00000475762.5:c.*1644A>G	ENSP00000432421.1:n.*1644A>G
ENST00000482007.5:c.*436A>G	ENSP00000433332.1:n.*436A>G
ENST00000487525.5:c.*584A>G	ENSP00000431637.1:n.*584A>G
ENST00000578151.1:n.240-1592A>G
ENST00000581221.5:n.523A>G
ENST00000583539.5:c.1008A>G	ENSP00000463121.1:p.Thr336=
ENST00000584804.1:c.242A>G	ENSP00000463658.1:p.Gln81Arg
NM_058216.2:c.1008A>G	NP_478123.1:p.Thr336=
NR_103872.1:n.912A>G
XM_006722001.2:c.1011A>G	XP_006722064.1:p.Thr337=
XM_006722002.2:c.947A>G	XP_006722065.1:p.Gln316Arg
XM_006722004.2:c.660A>G	XP_006722067.1:p.Thr220=
XM_006722005.2:c.660A>G	XP_006722068.1:p.Thr220=
XM_011525092.1:c.660A>G	XP_011523394.1:p.Thr220=
XM_011525093.1:c.660A>G	XP_011523395.1:p.Thr220=
XM_011525094.1:c.660A>G	XP_011523396.1:p.Thr220=
XR_934513.1:n.1226A>G
XR_934514.1:n.1229A>G
XR_934886.1:n.149+5545T>C
XM_006722001.4:c.1011A>G	XP_006722064.1:p.Thr337=
XM_006722002.4:c.947A>G	XP_006722065.1:p.Gln316Arg
XM_006722004.3:c.660A>G	XP_006722067.1:p.Thr220=
XM_006722005.3:c.660A>G	XP_006722068.1:p.Thr220=
XM_011525092.2:c.660A>G	XP_011523394.1:p.Thr220=
XM_011525093.2:c.660A>G	XP_011523395.1:p.Thr220=
XM_011525094.2:c.660A>G	XP_011523396.1:p.Thr220=
XM_017024914.1:c.657A>G	XP_016880403.1:p.Thr219=
XM_017024915.1:c.657A>G	XP_016880404.1:p.Thr219=
XM_017024916.1:c.657A>G	XP_016880405.1:p.Thr219=
XM_017024917.1:c.657A>G	XP_016880406.1:p.Thr219=
XM_017024918.2:c.657A>G	XP_016880407.1:p.Thr219=
XM_017024919.1:c.596A>G	XP_016880408.1:p.Gln199Arg
XR_934513.3:n.1657A>G
XR_934514.3:n.1660A>G
XR_934886.2:n.149+5545T>C
NM_058216.3:c.1008A>G MANE Select	NP_478123.1:p.Thr336=
NR_103872.2:n.883A>G