Canonical Allele Identifier: CA2267833068

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732369_58732372delinsAAAT , CM000679.2:g.58732369_58732372delinsAAAT	GRCh38
NC_000017.10:g.56809730_56809733delinsAAAT , CM000679.1:g.56809730_56809733delinsAAAT	GRCh37
NC_000017.9:g.54164729_54164732delinsAAAT	NCBI36
NG_023199.1:g.44768_44771delinsAAAT , LRG_314:g.44768_44771delinsAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.615-115_615-112delinsAAAT	ENSP00000464056.2:n.615-115_615-112delinsAAAT
ENST00000697680.1:c.*1930-115_*1930-112delinsAAAT	ENSP00000513392.1:n.*1930-115_*1930-112delinsAAAT
ENST00000697681.1:c.*2127-115_*2127-112delinsAAAT	ENSP00000513393.1:n.*2127-115_*2127-112delinsAAAT
ENST00000697683.1:c.*1902-115_*1902-112delinsAAAT	ENSP00000513395.1:n.*1902-115_*1902-112delinsAAAT
ENST00000697685.1:c.*1663-115_*1663-112delinsAAAT	ENSP00000513396.1:n.*1663-115_*1663-112delinsAAAT
ENST00000697686.1:c.737-115_737-112delinsAAAT	ENSP00000513397.1:n.737-115_737-112delinsAAAT
ENST00000697689.1:c.*1441-1749_*1441-1746delinsAAAT	ENSP00000513398.1:n.*1441-1749_*1441-1746delinsAAAT
ENST00000697690.1:c.905-1749_905-1746delinsAAAT	ENSP00000513399.1:n.905-1749_905-1746delinsAAAT
ENST00000697691.1:c.*938-115_*938-112delinsAAAT	ENSP00000513400.1:n.*938-115_*938-112delinsAAAT
ENST00000697692.1:c.*978-115_*978-112delinsAAAT	ENSP00000513401.1:n.*978-115_*978-112delinsAAAT
ENST00000697694.1:c.615-115_615-112delinsAAAT	ENSP00000513402.1:n.615-115_615-112delinsAAAT
ENST00000697695.1:n.1573-115_1573-112delinsAAAT
ENST00000337432.9:c.966-115_966-112delinsAAAT MANE Select	ENSP00000336701.4:n.966-115_966-112delinsAAAT
ENST00000337432.8:c.966-115_966-112delinsAAAT	ENSP00000336701.4:n.966-115_966-112delinsAAAT
ENST00000413590.5:c.604-112_604-109delinsAAAT
ENST00000461706.1:n.38_41delinsAAAT
ENST00000475762.5:c.*1602-115_*1602-112delinsAAAT	ENSP00000432421.1:n.*1602-115_*1602-112delinsAAAT
ENST00000482007.5:c.*394-115_*394-112delinsAAAT	ENSP00000433332.1:n.*394-115_*394-112delinsAAAT
ENST00000487525.5:c.*539-112_*539-109delinsAAAT	ENSP00000431637.1:n.*539-112_*539-109delinsAAAT
ENST00000578151.1:n.240-1749_240-1746delinsAAAT
ENST00000581221.5:n.481-115_481-112delinsAAAT
ENST00000583539.5:c.966-115_966-112delinsAAAT	ENSP00000463121.1:n.966-115_966-112delinsAAAT
ENST00000584617.5:c.688-115_688-112delinsAAAT
ENST00000584804.1:c.200-115_200-112delinsAAAT	ENSP00000463658.1:n.200-115_200-112delinsAAAT
NM_058216.2:c.966-115_966-112delinsAAAT	NP_478123.1:n.966-115_966-112delinsAAAT
NR_103872.1:n.870-115_870-112delinsAAAT
XM_006722001.2:c.966-112_966-109delinsAAAT	XP_006722064.1:n.966-112_966-109delinsAAAT
XM_006722002.2:c.905-115_905-112delinsAAAT	XP_006722065.1:n.905-115_905-112delinsAAAT
XM_006722004.2:c.615-112_615-109delinsAAAT	XP_006722067.1:n.615-112_615-109delinsAAAT
XM_006722005.2:c.615-112_615-109delinsAAAT	XP_006722068.1:n.615-112_615-109delinsAAAT
XM_011525092.1:c.615-112_615-109delinsAAAT	XP_011523394.1:n.615-112_615-109delinsAAAT
XM_011525093.1:c.615-112_615-109delinsAAAT	XP_011523395.1:n.615-112_615-109delinsAAAT
XM_011525094.1:c.615-112_615-109delinsAAAT	XP_011523396.1:n.615-112_615-109delinsAAAT
XR_934513.1:n.1184-115_1184-112delinsAAAT
XR_934514.1:n.1184-112_1184-109delinsAAAT
XR_934886.1:n.149+5699_149+5702delinsATTT
XM_006722001.4:c.966-112_966-109delinsAAAT	XP_006722064.1:n.966-112_966-109delinsAAAT
XM_006722002.4:c.905-115_905-112delinsAAAT	XP_006722065.1:n.905-115_905-112delinsAAAT
XM_006722004.3:c.615-112_615-109delinsAAAT	XP_006722067.1:n.615-112_615-109delinsAAAT
XM_006722005.3:c.615-112_615-109delinsAAAT	XP_006722068.1:n.615-112_615-109delinsAAAT
XM_011525092.2:c.615-112_615-109delinsAAAT	XP_011523394.1:n.615-112_615-109delinsAAAT
XM_011525093.2:c.615-112_615-109delinsAAAT	XP_011523395.1:n.615-112_615-109delinsAAAT
XM_011525094.2:c.615-112_615-109delinsAAAT	XP_011523396.1:n.615-112_615-109delinsAAAT
XM_017024914.1:c.615-115_615-112delinsAAAT	XP_016880403.1:n.615-115_615-112delinsAAAT
XM_017024915.1:c.615-115_615-112delinsAAAT	XP_016880404.1:n.615-115_615-112delinsAAAT
XM_017024916.1:c.615-115_615-112delinsAAAT	XP_016880405.1:n.615-115_615-112delinsAAAT
XM_017024917.1:c.615-115_615-112delinsAAAT	XP_016880406.1:n.615-115_615-112delinsAAAT
XM_017024918.2:c.615-115_615-112delinsAAAT	XP_016880407.1:n.615-115_615-112delinsAAAT
XM_017024919.1:c.554-115_554-112delinsAAAT	XP_016880408.1:n.554-115_554-112delinsAAAT
XR_934513.3:n.1615-115_1615-112delinsAAAT
XR_934514.3:n.1615-112_1615-109delinsAAAT
XR_934886.2:n.149+5699_149+5702delinsATTT
NM_058216.3:c.966-115_966-112delinsAAAT MANE Select	NP_478123.1:n.966-115_966-112delinsAAAT
NR_103872.2:n.841-115_841-112delinsAAAT