Canonical Allele Identifier: CA400364835

Gene: RAD51C

Linked Data

• dbSNP Id: rs747727600
• MyVariant Identifiers: chr17:g.56809846T>A (hg19) ; chr17:g.58732485T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732485T>A , CM000679.2:g.58732485T>A	GRCh38
NC_000017.10:g.56809846T>A , CM000679.1:g.56809846T>A	GRCh37
NC_000017.9:g.54164845T>A	NCBI36
NG_023199.1:g.44884T>A , LRG_314:g.44884T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.616T>A	ENSP00000464056.2:p.Leu206Met
ENST00000697680.1:c.*1931T>A	ENSP00000513392.1:n.*1931T>A
ENST00000697681.1:c.*2128T>A	ENSP00000513393.1:n.*2128T>A
ENST00000697683.1:c.*1903T>A	ENSP00000513395.1:n.*1903T>A
ENST00000697685.1:c.*1664T>A	ENSP00000513396.1:n.*1664T>A
ENST00000697686.1:c.738T>A	ENSP00000513397.1:p.Gly246=
ENST00000697689.1:c.*1441-1633T>A	ENSP00000513398.1:n.*1441-1633T>A
ENST00000697690.1:c.905-1633T>A	ENSP00000513399.1:n.905-1633T>A
ENST00000697691.1:c.*939T>A	ENSP00000513400.1:n.*939T>A
ENST00000697692.1:c.*979T>A	ENSP00000513401.1:n.*979T>A
ENST00000697694.1:c.616T>A	ENSP00000513402.1:p.Leu206Met
ENST00000697695.1:n.1574T>A
ENST00000337432.9:c.967T>A MANE Select	ENSP00000336701.4:p.Leu323Met
ENST00000337432.8:c.967T>A	ENSP00000336701.4:p.Leu323Met
ENST00000413590.5:c.608T>A
ENST00000461706.1:n.154T>A
ENST00000475762.5:c.*1603T>A	ENSP00000432421.1:n.*1603T>A
ENST00000482007.5:c.*395T>A	ENSP00000433332.1:n.*395T>A
ENST00000487525.5:c.*543T>A	ENSP00000431637.1:n.*543T>A
ENST00000578151.1:n.240-1633T>A
ENST00000581221.5:n.482T>A
ENST00000583539.5:c.967T>A	ENSP00000463121.1:p.Leu323Met
ENST00000584617.5:c.689T>A
ENST00000584804.1:c.201T>A	ENSP00000463658.1:p.Gly67=
NM_058216.2:c.967T>A	NP_478123.1:p.Leu323Met
NR_103872.1:n.871T>A
XM_006722001.2:c.970T>A	XP_006722064.1:p.Leu324Met
XM_006722002.2:c.906T>A	XP_006722065.1:p.Gly302=
XM_006722004.2:c.619T>A	XP_006722067.1:p.Leu207Met
XM_006722005.2:c.619T>A	XP_006722068.1:p.Leu207Met
XM_011525092.1:c.619T>A	XP_011523394.1:p.Leu207Met
XM_011525093.1:c.619T>A	XP_011523395.1:p.Leu207Met
XM_011525094.1:c.619T>A	XP_011523396.1:p.Leu207Met
XR_934513.1:n.1185T>A
XR_934514.1:n.1188T>A
XR_934886.1:n.149+5586A>T
XM_006722001.4:c.970T>A	XP_006722064.1:p.Leu324Met
XM_006722002.4:c.906T>A	XP_006722065.1:p.Gly302=
XM_006722004.3:c.619T>A	XP_006722067.1:p.Leu207Met
XM_006722005.3:c.619T>A	XP_006722068.1:p.Leu207Met
XM_011525092.2:c.619T>A	XP_011523394.1:p.Leu207Met
XM_011525093.2:c.619T>A	XP_011523395.1:p.Leu207Met
XM_011525094.2:c.619T>A	XP_011523396.1:p.Leu207Met
XM_017024914.1:c.616T>A	XP_016880403.1:p.Leu206Met
XM_017024915.1:c.616T>A	XP_016880404.1:p.Leu206Met
XM_017024916.1:c.616T>A	XP_016880405.1:p.Leu206Met
XM_017024917.1:c.616T>A	XP_016880406.1:p.Leu206Met
XM_017024918.2:c.616T>A	XP_016880407.1:p.Leu206Met
XM_017024919.1:c.555T>A	XP_016880408.1:p.Gly185=
XR_934513.3:n.1616T>A
XR_934514.3:n.1619T>A
XR_934886.2:n.149+5586A>T
NM_058216.3:c.967T>A MANE Select	NP_478123.1:p.Leu323Met
NR_103872.2:n.842T>A