Canonical Allele Identifier: CA2267833143
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732459_58732463delinsGTATT , CM000679.2:g.58732459_58732463delinsGTATT GRCh38
NC_000017.10:g.56809820_56809824delinsGTATT , CM000679.1:g.56809820_56809824delinsGTATT GRCh37
NC_000017.9:g.54164819_54164823delinsGTATT NCBI36
NG_023199.1:g.44858_44862delinsGTATT , LRG_314:g.44858_44862delinsGTATT

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.615-25_615-21delinsGTATT ENSP00000464056.2:n.615-25_615-21delinsGT...
ENST00000697680.1:c.*1930-25_*1930-21delinsGTATT ENSP00000513392.1:n.*1930-25_*1930-21deli...
ENST00000697681.1:c.*2127-25_*2127-21delinsGTATT ENSP00000513393.1:n.*2127-25_*2127-21deli...
ENST00000697683.1:c.*1902-25_*1902-21delinsGTATT ENSP00000513395.1:n.*1902-25_*1902-21deli...
ENST00000697685.1:c.*1663-25_*1663-21delinsGTATT ENSP00000513396.1:n.*1663-25_*1663-21deli...
ENST00000697686.1:c.737-25_737-21delinsGTATT ENSP00000513397.1:n.737-25_737-21delinsGT...
ENST00000697689.1:c.*1441-1659_*1441-1655delinsGTATT ENSP00000513398.1:n.*1441-1659_*1441-1655...
ENST00000697690.1:c.905-1659_905-1655delinsGTATT ENSP00000513399.1:n.905-1659_905-1655deli...
ENST00000697691.1:c.*938-25_*938-21delinsGTATT ENSP00000513400.1:n.*938-25_*938-21delins...
ENST00000697692.1:c.*978-25_*978-21delinsGTATT ENSP00000513401.1:n.*978-25_*978-21delins...
ENST00000697694.1:c.615-25_615-21delinsGTATT ENSP00000513402.1:n.615-25_615-21delinsGT...
ENST00000697695.1:n.1573-25_1573-21delinsGTATT
ENST00000337432.9:c.966-25_966-21delinsGTATT MANE Select ENSP00000336701.4:n.966-25_966-21delinsGT...
ENST00000337432.8:c.966-25_966-21delinsGTATT ENSP00000336701.4:n.966-25_966-21delinsGT...
ENST00000413590.5:c.604-22_604-18delinsGTATT
ENST00000461706.1:n.128_132delinsGTATT
ENST00000475762.5:c.*1602-25_*1602-21delinsGTATT ENSP00000432421.1:n.*1602-25_*1602-21deli...
ENST00000482007.5:c.*394-25_*394-21delinsGTATT ENSP00000433332.1:n.*394-25_*394-21delins...
ENST00000487525.5:c.*539-22_*539-18delinsGTATT ENSP00000431637.1:n.*539-22_*539-18delins...
ENST00000578151.1:n.240-1659_240-1655delinsGTATT
ENST00000581221.5:n.481-25_481-21delinsGTATT
ENST00000583539.5:c.966-25_966-21delinsGTATT ENSP00000463121.1:n.966-25_966-21delinsGT...
ENST00000584617.5:c.688-25_688-21delinsGTATT
ENST00000584804.1:c.200-25_200-21delinsGTATT ENSP00000463658.1:n.200-25_200-21delinsGT...
NM_058216.2:c.966-25_966-21delinsGTATT NP_478123.1:n.966-25_966-21delinsGTATT
NR_103872.1:n.870-25_870-21delinsGTATT
XM_006722001.2:c.966-22_966-18delinsGTATT XP_006722064.1:n.966-22_966-18delinsGTATT...
XM_006722002.2:c.905-25_905-21delinsGTATT XP_006722065.1:n.905-25_905-21delinsGTATT...
XM_006722004.2:c.615-22_615-18delinsGTATT XP_006722067.1:n.615-22_615-18delinsGTATT...
XM_006722005.2:c.615-22_615-18delinsGTATT XP_006722068.1:n.615-22_615-18delinsGTATT...
XM_011525092.1:c.615-22_615-18delinsGTATT XP_011523394.1:n.615-22_615-18delinsGTATT...
XM_011525093.1:c.615-22_615-18delinsGTATT XP_011523395.1:n.615-22_615-18delinsGTATT...
XM_011525094.1:c.615-22_615-18delinsGTATT XP_011523396.1:n.615-22_615-18delinsGTATT...
XR_934513.1:n.1184-25_1184-21delinsGTATT
XR_934514.1:n.1184-22_1184-18delinsGTATT
XR_934886.1:n.149+5608_149+5612delinsAATAC
XM_006722001.4:c.966-22_966-18delinsGTATT XP_006722064.1:n.966-22_966-18delinsGTATT...
XM_006722002.4:c.905-25_905-21delinsGTATT XP_006722065.1:n.905-25_905-21delinsGTATT...
XM_006722004.3:c.615-22_615-18delinsGTATT XP_006722067.1:n.615-22_615-18delinsGTATT...
XM_006722005.3:c.615-22_615-18delinsGTATT XP_006722068.1:n.615-22_615-18delinsGTATT...
XM_011525092.2:c.615-22_615-18delinsGTATT XP_011523394.1:n.615-22_615-18delinsGTATT...
XM_011525093.2:c.615-22_615-18delinsGTATT XP_011523395.1:n.615-22_615-18delinsGTATT...
XM_011525094.2:c.615-22_615-18delinsGTATT XP_011523396.1:n.615-22_615-18delinsGTATT...
XM_017024914.1:c.615-25_615-21delinsGTATT XP_016880403.1:n.615-25_615-21delinsGTATT...
XM_017024915.1:c.615-25_615-21delinsGTATT XP_016880404.1:n.615-25_615-21delinsGTATT...
XM_017024916.1:c.615-25_615-21delinsGTATT XP_016880405.1:n.615-25_615-21delinsGTATT...
XM_017024917.1:c.615-25_615-21delinsGTATT XP_016880406.1:n.615-25_615-21delinsGTATT...
XM_017024918.2:c.615-25_615-21delinsGTATT XP_016880407.1:n.615-25_615-21delinsGTATT...
XM_017024919.1:c.554-25_554-21delinsGTATT XP_016880408.1:n.554-25_554-21delinsGTATT...
XR_934513.3:n.1615-25_1615-21delinsGTATT
XR_934514.3:n.1615-22_1615-18delinsGTATT
XR_934886.2:n.149+5608_149+5612delinsAATAC
NM_058216.3:c.966-25_966-21delinsGTATT MANE Select NP_478123.1:n.966-25_966-21delinsGTATT
NR_103872.2:n.841-25_841-21delinsGTATT