Canonical Allele Identifier: CA2809986050

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732377_58732381del , CM000679.2:g.58732377_58732381del	GRCh38
NC_000017.10:g.56809738_56809742del , CM000679.1:g.56809738_56809742del	GRCh37
NC_000017.9:g.54164737_54164741del	NCBI36
NG_023199.1:g.44776_44780del , LRG_314:g.44776_44780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.615-107_615-103del	ENSP00000464056.2:n.615-107_615-103del
ENST00000697680.1:c.*1930-107_*1930-103del	ENSP00000513392.1:n.*1930-107_*1930-103del
ENST00000697681.1:c.*2127-107_*2127-103del	ENSP00000513393.1:n.*2127-107_*2127-103del
ENST00000697683.1:c.*1902-107_*1902-103del	ENSP00000513395.1:n.*1902-107_*1902-103del
ENST00000697685.1:c.*1663-107_*1663-103del	ENSP00000513396.1:n.*1663-107_*1663-103del
ENST00000697686.1:c.737-107_737-103del	ENSP00000513397.1:n.737-107_737-103del
ENST00000697689.1:c.*1441-1741_*1441-1737del	ENSP00000513398.1:n.*1441-1741_*1441-1737del
ENST00000697690.1:c.905-1741_905-1737del	ENSP00000513399.1:n.905-1741_905-1737del
ENST00000697691.1:c.*938-107_*938-103del	ENSP00000513400.1:n.*938-107_*938-103del
ENST00000697692.1:c.*978-107_*978-103del	ENSP00000513401.1:n.*978-107_*978-103del
ENST00000697694.1:c.615-107_615-103del	ENSP00000513402.1:n.615-107_615-103del
ENST00000697695.1:n.1573-107_1573-103del
ENST00000337432.9:c.966-107_966-103del MANE Select	ENSP00000336701.4:n.966-107_966-103del
ENST00000337432.8:c.966-107_966-103del	ENSP00000336701.4:n.966-107_966-103del
ENST00000413590.5:c.604-104_604-100del
ENST00000461706.1:n.46_50del
ENST00000475762.5:c.*1602-107_*1602-103del	ENSP00000432421.1:n.*1602-107_*1602-103del
ENST00000482007.5:c.*394-107_*394-103del	ENSP00000433332.1:n.*394-107_*394-103del
ENST00000487525.5:c.*539-104_*539-100del	ENSP00000431637.1:n.*539-104_*539-100del
ENST00000578151.1:n.240-1741_240-1737del
ENST00000581221.5:n.481-107_481-103del
ENST00000583539.5:c.966-107_966-103del	ENSP00000463121.1:n.966-107_966-103del
ENST00000584617.5:c.688-107_688-103del
ENST00000584804.1:c.200-107_200-103del	ENSP00000463658.1:n.200-107_200-103del
NM_058216.2:c.966-107_966-103del	NP_478123.1:n.966-107_966-103del
NR_103872.1:n.870-107_870-103del
XM_006722001.2:c.966-104_966-100del	XP_006722064.1:n.966-104_966-100del
XM_006722002.2:c.905-107_905-103del	XP_006722065.1:n.905-107_905-103del
XM_006722004.2:c.615-104_615-100del	XP_006722067.1:n.615-104_615-100del
XM_006722005.2:c.615-104_615-100del	XP_006722068.1:n.615-104_615-100del
XM_011525092.1:c.615-104_615-100del	XP_011523394.1:n.615-104_615-100del
XM_011525093.1:c.615-104_615-100del	XP_011523395.1:n.615-104_615-100del
XM_011525094.1:c.615-104_615-100del	XP_011523396.1:n.615-104_615-100del
XR_934513.1:n.1184-107_1184-103del
XR_934514.1:n.1184-104_1184-100del
XR_934886.1:n.149+5690_149+5694del
XM_006722001.4:c.966-104_966-100del	XP_006722064.1:n.966-104_966-100del
XM_006722002.4:c.905-107_905-103del	XP_006722065.1:n.905-107_905-103del
XM_006722004.3:c.615-104_615-100del	XP_006722067.1:n.615-104_615-100del
XM_006722005.3:c.615-104_615-100del	XP_006722068.1:n.615-104_615-100del
XM_011525092.2:c.615-104_615-100del	XP_011523394.1:n.615-104_615-100del
XM_011525093.2:c.615-104_615-100del	XP_011523395.1:n.615-104_615-100del
XM_011525094.2:c.615-104_615-100del	XP_011523396.1:n.615-104_615-100del
XM_017024914.1:c.615-107_615-103del	XP_016880403.1:n.615-107_615-103del
XM_017024915.1:c.615-107_615-103del	XP_016880404.1:n.615-107_615-103del
XM_017024916.1:c.615-107_615-103del	XP_016880405.1:n.615-107_615-103del
XM_017024917.1:c.615-107_615-103del	XP_016880406.1:n.615-107_615-103del
XM_017024918.2:c.615-107_615-103del	XP_016880407.1:n.615-107_615-103del
XM_017024919.1:c.554-107_554-103del	XP_016880408.1:n.554-107_554-103del
XR_934513.3:n.1615-107_1615-103del
XR_934514.3:n.1615-104_1615-100del
XR_934886.2:n.149+5690_149+5694del
NM_058216.3:c.966-107_966-103del MANE Select	NP_478123.1:n.966-107_966-103del
NR_103872.2:n.841-107_841-103del