Canonical Allele Identifier: CA8677378
Gene: RAD51C HGNC NCBI

Linked Data

dbSNP Id: rs750713657

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732464_58732467del , CM000679.2:g.58732464_58732467del GRCh38
NC_000017.10:g.56809825_56809828del , CM000679.1:g.56809825_56809828del GRCh37
NC_000017.9:g.54164824_54164827del NCBI36
NG_023199.1:g.44863_44866del , LRG_314:g.44863_44866del

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.615-20_615-17del ENSP00000464056.2:n.615-20_615-17del
ENST00000697680.1:c.*1930-20_*1930-17del ENSP00000513392.1:n.*1930-20_*1930-17del
ENST00000697681.1:c.*2127-20_*2127-17del ENSP00000513393.1:n.*2127-20_*2127-17del
ENST00000697683.1:c.*1902-20_*1902-17del ENSP00000513395.1:n.*1902-20_*1902-17del
ENST00000697685.1:c.*1663-20_*1663-17del ENSP00000513396.1:n.*1663-20_*1663-17del
ENST00000697686.1:c.737-20_737-17del ENSP00000513397.1:n.737-20_737-17del
ENST00000697689.1:c.*1441-1654_*1441-1651del ENSP00000513398.1:n.*1441-1654_*1441-1651...
ENST00000697690.1:c.905-1654_905-1651del ENSP00000513399.1:n.905-1654_905-1651del
ENST00000697691.1:c.*938-20_*938-17del ENSP00000513400.1:n.*938-20_*938-17del
ENST00000697692.1:c.*978-20_*978-17del ENSP00000513401.1:n.*978-20_*978-17del
ENST00000697694.1:c.615-20_615-17del ENSP00000513402.1:n.615-20_615-17del
ENST00000697695.1:n.1573-20_1573-17del
ENST00000337432.9:c.966-20_966-17del MANE Select ENSP00000336701.4:n.966-20_966-17del
ENST00000337432.8:c.966-20_966-17del ENSP00000336701.4:n.966-20_966-17del
ENST00000413590.5:c.604-17_604-14del
ENST00000461706.1:n.133_136del
ENST00000475762.5:c.*1602-20_*1602-17del ENSP00000432421.1:n.*1602-20_*1602-17del
ENST00000482007.5:c.*394-20_*394-17del ENSP00000433332.1:n.*394-20_*394-17del
ENST00000487525.5:c.*539-17_*539-14del ENSP00000431637.1:n.*539-17_*539-14del
ENST00000578151.1:n.240-1654_240-1651del
ENST00000581221.5:n.481-20_481-17del
ENST00000583539.5:c.966-20_966-17del ENSP00000463121.1:n.966-20_966-17del
ENST00000584617.5:c.688-20_688-17del
ENST00000584804.1:c.200-20_200-17del ENSP00000463658.1:n.200-20_200-17del
NM_058216.2:c.966-20_966-17del NP_478123.1:n.966-20_966-17del
NR_103872.1:n.870-20_870-17del
XM_006722001.2:c.966-17_966-14del XP_006722064.1:n.966-17_966-14del
XM_006722002.2:c.905-20_905-17del XP_006722065.1:n.905-20_905-17del
XM_006722004.2:c.615-17_615-14del XP_006722067.1:n.615-17_615-14del
XM_006722005.2:c.615-17_615-14del XP_006722068.1:n.615-17_615-14del
XM_011525092.1:c.615-17_615-14del XP_011523394.1:n.615-17_615-14del
XM_011525093.1:c.615-17_615-14del XP_011523395.1:n.615-17_615-14del
XM_011525094.1:c.615-17_615-14del XP_011523396.1:n.615-17_615-14del
XR_934513.1:n.1184-20_1184-17del
XR_934514.1:n.1184-17_1184-14del
XR_934886.1:n.149+5608_149+5611del
XM_006722001.4:c.966-17_966-14del XP_006722064.1:n.966-17_966-14del
XM_006722002.4:c.905-20_905-17del XP_006722065.1:n.905-20_905-17del
XM_006722004.3:c.615-17_615-14del XP_006722067.1:n.615-17_615-14del
XM_006722005.3:c.615-17_615-14del XP_006722068.1:n.615-17_615-14del
XM_011525092.2:c.615-17_615-14del XP_011523394.1:n.615-17_615-14del
XM_011525093.2:c.615-17_615-14del XP_011523395.1:n.615-17_615-14del
XM_011525094.2:c.615-17_615-14del XP_011523396.1:n.615-17_615-14del
XM_017024914.1:c.615-20_615-17del XP_016880403.1:n.615-20_615-17del
XM_017024915.1:c.615-20_615-17del XP_016880404.1:n.615-20_615-17del
XM_017024916.1:c.615-20_615-17del XP_016880405.1:n.615-20_615-17del
XM_017024917.1:c.615-20_615-17del XP_016880406.1:n.615-20_615-17del
XM_017024918.2:c.615-20_615-17del XP_016880407.1:n.615-20_615-17del
XM_017024919.1:c.554-20_554-17del XP_016880408.1:n.554-20_554-17del
XR_934513.3:n.1615-20_1615-17del
XR_934514.3:n.1615-17_1615-14del
XR_934886.2:n.149+5608_149+5611del
NM_058216.3:c.966-20_966-17del MANE Select NP_478123.1:n.966-20_966-17del
NR_103872.2:n.841-20_841-17del