Canonical Allele Identifier: CA10580764

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 231694
• ClinVar RCV Id: RCV000216715 ; RCV001485533 ; RCV003477735
• dbSNP Id: rs876659303
• gnomAD v4: 17-58732505-A-T
• MyVariant Identifiers: chr17:g.56809866A>T (hg19) ; chr17:g.58732505A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732505A>T , CM000679.2:g.58732505A>T	GRCh38
NC_000017.10:g.56809866A>T , CM000679.1:g.56809866A>T	GRCh37
NC_000017.9:g.54164865A>T	NCBI36
NG_023199.1:g.44904A>T , LRG_314:g.44904A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.636A>T	ENSP00000464056.2:p.Ser212=
ENST00000697680.1:c.*1951A>T	ENSP00000513392.1:n.*1951A>T
ENST00000697681.1:c.*2148A>T	ENSP00000513393.1:n.*2148A>T
ENST00000697683.1:c.*1923A>T	ENSP00000513395.1:n.*1923A>T
ENST00000697685.1:c.*1684A>T	ENSP00000513396.1:n.*1684A>T
ENST00000697686.1:c.758A>T	ENSP00000513397.1:p.His253Leu
ENST00000697689.1:c.*1441-1613A>T	ENSP00000513398.1:n.*1441-1613A>T
ENST00000697690.1:c.905-1613A>T	ENSP00000513399.1:n.905-1613A>T
ENST00000697691.1:c.*959A>T	ENSP00000513400.1:n.*959A>T
ENST00000697692.1:c.*999A>T	ENSP00000513401.1:n.*999A>T
ENST00000697694.1:c.636A>T	ENSP00000513402.1:p.Ser212=
ENST00000697695.1:n.1594A>T
ENST00000337432.9:c.987A>T MANE Select	ENSP00000336701.4:p.Ser329=
ENST00000337432.8:c.987A>T	ENSP00000336701.4:p.Ser329=
ENST00000413590.5:c.628A>T
ENST00000461706.1:n.174A>T
ENST00000475762.5:c.*1623A>T	ENSP00000432421.1:n.*1623A>T
ENST00000482007.5:c.*415A>T	ENSP00000433332.1:n.*415A>T
ENST00000487525.5:c.*563A>T	ENSP00000431637.1:n.*563A>T
ENST00000578151.1:n.240-1613A>T
ENST00000581221.5:n.502A>T
ENST00000583539.5:c.987A>T	ENSP00000463121.1:p.Ser329=
ENST00000584617.5:c.709A>T
ENST00000584804.1:c.221A>T	ENSP00000463658.1:p.His74Leu
NM_058216.2:c.987A>T	NP_478123.1:p.Ser329=
NR_103872.1:n.891A>T
XM_006722001.2:c.990A>T	XP_006722064.1:p.Ser330=
XM_006722002.2:c.926A>T	XP_006722065.1:p.His309Leu
XM_006722004.2:c.639A>T	XP_006722067.1:p.Ser213=
XM_006722005.2:c.639A>T	XP_006722068.1:p.Ser213=
XM_011525092.1:c.639A>T	XP_011523394.1:p.Ser213=
XM_011525093.1:c.639A>T	XP_011523395.1:p.Ser213=
XM_011525094.1:c.639A>T	XP_011523396.1:p.Ser213=
XR_934513.1:n.1205A>T
XR_934514.1:n.1208A>T
XR_934886.1:n.149+5566T>A
XM_006722001.4:c.990A>T	XP_006722064.1:p.Ser330=
XM_006722002.4:c.926A>T	XP_006722065.1:p.His309Leu
XM_006722004.3:c.639A>T	XP_006722067.1:p.Ser213=
XM_006722005.3:c.639A>T	XP_006722068.1:p.Ser213=
XM_011525092.2:c.639A>T	XP_011523394.1:p.Ser213=
XM_011525093.2:c.639A>T	XP_011523395.1:p.Ser213=
XM_011525094.2:c.639A>T	XP_011523396.1:p.Ser213=
XM_017024914.1:c.636A>T	XP_016880403.1:p.Ser212=
XM_017024915.1:c.636A>T	XP_016880404.1:p.Ser212=
XM_017024916.1:c.636A>T	XP_016880405.1:p.Ser212=
XM_017024917.1:c.636A>T	XP_016880406.1:p.Ser212=
XM_017024918.2:c.636A>T	XP_016880407.1:p.Ser212=
XM_017024919.1:c.575A>T	XP_016880408.1:p.His192Leu
XR_934513.3:n.1636A>T
XR_934514.3:n.1639A>T
XR_934886.2:n.149+5566T>A
NM_058216.3:c.987A>T MANE Select	NP_478123.1:p.Ser329=
NR_103872.2:n.862A>T