Canonical Allele Identifier: CA501075581

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56787282T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709921T>C , CM000679.2:g.58709921T>C	GRCh38
NC_000017.10:g.56787282T>C , CM000679.1:g.56787282T>C	GRCh37
NC_000017.9:g.54142281T>C	NCBI36
NG_023199.1:g.22320T>C , LRG_314:g.22320T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.417T>C	ENSP00000464056.2:p.Ser139=
ENST00000697678.1:n.670T>C
ENST00000697679.1:n.1842T>C
ENST00000697680.1:c.*1632T>C	ENSP00000513392.1:n.*1632T>C
ENST00000697681.1:c.*1929T>C	ENSP00000513393.1:n.*1929T>C
ENST00000697683.1:c.*1632T>C	ENSP00000513395.1:n.*1632T>C
ENST00000697684.1:n.828T>C
ENST00000697685.1:c.*1465T>C	ENSP00000513396.1:n.*1465T>C
ENST00000697686.1:c.417T>C	ENSP00000513397.1:p.Ser139=
ENST00000697687.1:n.647T>C
ENST00000697688.1:n.814T>C
ENST00000697689.1:c.*1304T>C	ENSP00000513398.1:n.*1304T>C
ENST00000697690.1:c.768T>C	ENSP00000513399.1:p.Ser256=
ENST00000697691.1:c.*740T>C	ENSP00000513400.1:n.*740T>C
ENST00000697692.1:c.*780T>C	ENSP00000513401.1:n.*780T>C
ENST00000697694.1:c.417T>C	ENSP00000513402.1:p.Ser139=
ENST00000697695.1:n.1375T>C
ENST00000337432.9:c.768T>C MANE Select	ENSP00000336701.4:p.Ser256=
ENST00000337432.8:c.768T>C	ENSP00000336701.4:p.Ser256=
ENST00000413590.5:c.406T>C
ENST00000475762.5:c.*1471T>C	ENSP00000432421.1:n.*1471T>C
ENST00000482007.5:c.*196T>C	ENSP00000433332.1:n.*196T>C
ENST00000487525.5:c.*341T>C	ENSP00000431637.1:n.*341T>C
ENST00000578151.1:n.103T>C
ENST00000581221.5:n.283T>C
ENST00000583539.5:c.768T>C	ENSP00000463121.1:p.Ser256=
ENST00000584617.5:c.490T>C
ENST00000584804.1:c.63T>C	ENSP00000463658.1:p.Ser21=
NM_058216.2:c.768T>C	NP_478123.1:p.Ser256=
NR_103872.1:n.672T>C
XM_006722001.2:c.768T>C	XP_006722064.1:p.Ser256=
XM_006722002.2:c.768T>C	XP_006722065.1:p.Ser256=
XM_006722004.2:c.417T>C	XP_006722067.1:p.Ser139=
XM_006722005.2:c.417T>C	XP_006722068.1:p.Ser139=
XM_011525092.1:c.417T>C	XP_011523394.1:p.Ser139=
XM_011525093.1:c.417T>C	XP_011523395.1:p.Ser139=
XM_011525094.1:c.417T>C	XP_011523396.1:p.Ser139=
XR_934513.1:n.986T>C
XR_934514.1:n.986T>C
XM_006722001.4:c.768T>C	XP_006722064.1:p.Ser256=
XM_006722002.4:c.768T>C	XP_006722065.1:p.Ser256=
XM_006722004.3:c.417T>C	XP_006722067.1:p.Ser139=
XM_006722005.3:c.417T>C	XP_006722068.1:p.Ser139=
XM_011525092.2:c.417T>C	XP_011523394.1:p.Ser139=
XM_011525093.2:c.417T>C	XP_011523395.1:p.Ser139=
XM_011525094.2:c.417T>C	XP_011523396.1:p.Ser139=
XM_017024914.1:c.417T>C	XP_016880403.1:p.Ser139=
XM_017024915.1:c.417T>C	XP_016880404.1:p.Ser139=
XM_017024916.1:c.417T>C	XP_016880405.1:p.Ser139=
XM_017024917.1:c.417T>C	XP_016880406.1:p.Ser139=
XM_017024918.2:c.417T>C	XP_016880407.1:p.Ser139=
XM_017024919.1:c.417T>C	XP_016880408.1:p.Ser139=
XR_934513.3:n.1417T>C
XR_934514.3:n.1417T>C
NM_058216.3:c.768T>C MANE Select	NP_478123.1:p.Ser256=
NR_103872.2:n.643T>C