Canonical Allele Identifier: CA2733814050

Gene: RAD51C

Linked Data

• dbSNP Id: rs2144043350

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732459_58732462del , CM000679.2:g.58732459_58732462del	GRCh38
NC_000017.10:g.56809820_56809823del , CM000679.1:g.56809820_56809823del	GRCh37
NC_000017.9:g.54164819_54164822del	NCBI36
NG_023199.1:g.44858_44861del , LRG_314:g.44858_44861del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.615-25_615-22del	ENSP00000464056.2:n.615-25_615-22del
ENST00000697680.1:c.*1930-25_*1930-22del	ENSP00000513392.1:n.*1930-25_*1930-22del
ENST00000697681.1:c.*2127-25_*2127-22del	ENSP00000513393.1:n.*2127-25_*2127-22del
ENST00000697683.1:c.*1902-25_*1902-22del	ENSP00000513395.1:n.*1902-25_*1902-22del
ENST00000697685.1:c.*1663-25_*1663-22del	ENSP00000513396.1:n.*1663-25_*1663-22del
ENST00000697686.1:c.737-25_737-22del	ENSP00000513397.1:n.737-25_737-22del
ENST00000697689.1:c.*1441-1659_*1441-1656del	ENSP00000513398.1:n.*1441-1659_*1441-1656...
ENST00000697690.1:c.905-1659_905-1656del	ENSP00000513399.1:n.905-1659_905-1656del
ENST00000697691.1:c.*938-25_*938-22del	ENSP00000513400.1:n.*938-25_*938-22del
ENST00000697692.1:c.*978-25_*978-22del	ENSP00000513401.1:n.*978-25_*978-22del
ENST00000697694.1:c.615-25_615-22del	ENSP00000513402.1:n.615-25_615-22del
ENST00000697695.1:n.1573-25_1573-22del
ENST00000337432.9:c.966-25_966-22del MANE Select	ENSP00000336701.4:n.966-25_966-22del
ENST00000337432.8:c.966-25_966-22del	ENSP00000336701.4:n.966-25_966-22del
ENST00000413590.5:c.604-22_604-19del
ENST00000461706.1:n.128_131del
ENST00000475762.5:c.*1602-25_*1602-22del	ENSP00000432421.1:n.*1602-25_*1602-22del
ENST00000482007.5:c.*394-25_*394-22del	ENSP00000433332.1:n.*394-25_*394-22del
ENST00000487525.5:c.*539-22_*539-19del	ENSP00000431637.1:n.*539-22_*539-19del
ENST00000578151.1:n.240-1659_240-1656del
ENST00000581221.5:n.481-25_481-22del
ENST00000583539.5:c.966-25_966-22del	ENSP00000463121.1:n.966-25_966-22del
ENST00000584617.5:c.688-25_688-22del
ENST00000584804.1:c.200-25_200-22del	ENSP00000463658.1:n.200-25_200-22del
NM_058216.2:c.966-25_966-22del	NP_478123.1:n.966-25_966-22del
NR_103872.1:n.870-25_870-22del
XM_006722001.2:c.966-22_966-19del	XP_006722064.1:n.966-22_966-19del
XM_006722002.2:c.905-25_905-22del	XP_006722065.1:n.905-25_905-22del
XM_006722004.2:c.615-22_615-19del	XP_006722067.1:n.615-22_615-19del
XM_006722005.2:c.615-22_615-19del	XP_006722068.1:n.615-22_615-19del
XM_011525092.1:c.615-22_615-19del	XP_011523394.1:n.615-22_615-19del
XM_011525093.1:c.615-22_615-19del	XP_011523395.1:n.615-22_615-19del
XM_011525094.1:c.615-22_615-19del	XP_011523396.1:n.615-22_615-19del
XR_934513.1:n.1184-25_1184-22del
XR_934514.1:n.1184-22_1184-19del
XR_934886.1:n.149+5614_149+5617del
XM_006722001.4:c.966-22_966-19del	XP_006722064.1:n.966-22_966-19del
XM_006722002.4:c.905-25_905-22del	XP_006722065.1:n.905-25_905-22del
XM_006722004.3:c.615-22_615-19del	XP_006722067.1:n.615-22_615-19del
XM_006722005.3:c.615-22_615-19del	XP_006722068.1:n.615-22_615-19del
XM_011525092.2:c.615-22_615-19del	XP_011523394.1:n.615-22_615-19del
XM_011525093.2:c.615-22_615-19del	XP_011523395.1:n.615-22_615-19del
XM_011525094.2:c.615-22_615-19del	XP_011523396.1:n.615-22_615-19del
XM_017024914.1:c.615-25_615-22del	XP_016880403.1:n.615-25_615-22del
XM_017024915.1:c.615-25_615-22del	XP_016880404.1:n.615-25_615-22del
XM_017024916.1:c.615-25_615-22del	XP_016880405.1:n.615-25_615-22del
XM_017024917.1:c.615-25_615-22del	XP_016880406.1:n.615-25_615-22del
XM_017024918.2:c.615-25_615-22del	XP_016880407.1:n.615-25_615-22del
XM_017024919.1:c.554-25_554-22del	XP_016880408.1:n.554-25_554-22del
XR_934513.3:n.1615-25_1615-22del
XR_934514.3:n.1615-22_1615-19del
XR_934886.2:n.149+5614_149+5617del
NM_058216.3:c.966-25_966-22del MANE Select	NP_478123.1:n.966-25_966-22del
NR_103872.2:n.841-25_841-22del