Canonical Allele Identifier: CA2267833139
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732451_58732452delinsGT , CM000679.2:g.58732451_58732452delinsGT GRCh38
NC_000017.10:g.56809812_56809813delinsGT , CM000679.1:g.56809812_56809813delinsGT GRCh37
NC_000017.9:g.54164811_54164812delinsGT NCBI36
NG_023199.1:g.44850_44851delinsGT , LRG_314:g.44850_44851delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.615-33_615-32delinsGT ENSP00000464056.2:n.615-33_615-32delinsGT...
ENST00000697680.1:c.*1930-33_*1930-32delinsGT ENSP00000513392.1:n.*1930-33_*1930-32deli...
ENST00000697681.1:c.*2127-33_*2127-32delinsGT ENSP00000513393.1:n.*2127-33_*2127-32deli...
ENST00000697683.1:c.*1902-33_*1902-32delinsGT ENSP00000513395.1:n.*1902-33_*1902-32deli...
ENST00000697685.1:c.*1663-33_*1663-32delinsGT ENSP00000513396.1:n.*1663-33_*1663-32deli...
ENST00000697686.1:c.737-33_737-32delinsGT ENSP00000513397.1:n.737-33_737-32delinsGT...
ENST00000697689.1:c.*1441-1667_*1441-1666delinsGT ENSP00000513398.1:n.*1441-1667_*1441-1666...
ENST00000697690.1:c.905-1667_905-1666delinsGT ENSP00000513399.1:n.905-1667_905-1666deli...
ENST00000697691.1:c.*938-33_*938-32delinsGT ENSP00000513400.1:n.*938-33_*938-32delins...
ENST00000697692.1:c.*978-33_*978-32delinsGT ENSP00000513401.1:n.*978-33_*978-32delins...
ENST00000697694.1:c.615-33_615-32delinsGT ENSP00000513402.1:n.615-33_615-32delinsGT...
ENST00000697695.1:n.1573-33_1573-32delinsGT
ENST00000337432.9:c.966-33_966-32delinsGT MANE Select ENSP00000336701.4:n.966-33_966-32delinsGT...
ENST00000337432.8:c.966-33_966-32delinsGT ENSP00000336701.4:n.966-33_966-32delinsGT...
ENST00000413590.5:c.604-30_604-29delinsGT
ENST00000461706.1:n.120_121delinsGT
ENST00000475762.5:c.*1602-33_*1602-32delinsGT ENSP00000432421.1:n.*1602-33_*1602-32deli...
ENST00000482007.5:c.*394-33_*394-32delinsGT ENSP00000433332.1:n.*394-33_*394-32delins...
ENST00000487525.5:c.*539-30_*539-29delinsGT ENSP00000431637.1:n.*539-30_*539-29delins...
ENST00000578151.1:n.240-1667_240-1666delinsGT
ENST00000581221.5:n.481-33_481-32delinsGT
ENST00000583539.5:c.966-33_966-32delinsGT ENSP00000463121.1:n.966-33_966-32delinsGT...
ENST00000584617.5:c.688-33_688-32delinsGT
ENST00000584804.1:c.200-33_200-32delinsGT ENSP00000463658.1:n.200-33_200-32delinsGT...
NM_058216.2:c.966-33_966-32delinsGT NP_478123.1:n.966-33_966-32delinsGT
NR_103872.1:n.870-33_870-32delinsGT
XM_006722001.2:c.966-30_966-29delinsGT XP_006722064.1:n.966-30_966-29delinsGT
XM_006722002.2:c.905-33_905-32delinsGT XP_006722065.1:n.905-33_905-32delinsGT
XM_006722004.2:c.615-30_615-29delinsGT XP_006722067.1:n.615-30_615-29delinsGT
XM_006722005.2:c.615-30_615-29delinsGT XP_006722068.1:n.615-30_615-29delinsGT
XM_011525092.1:c.615-30_615-29delinsGT XP_011523394.1:n.615-30_615-29delinsGT
XM_011525093.1:c.615-30_615-29delinsGT XP_011523395.1:n.615-30_615-29delinsGT
XM_011525094.1:c.615-30_615-29delinsGT XP_011523396.1:n.615-30_615-29delinsGT
XR_934513.1:n.1184-33_1184-32delinsGT
XR_934514.1:n.1184-30_1184-29delinsGT
XR_934886.1:n.149+5619_149+5620delinsAC
XM_006722001.4:c.966-30_966-29delinsGT XP_006722064.1:n.966-30_966-29delinsGT
XM_006722002.4:c.905-33_905-32delinsGT XP_006722065.1:n.905-33_905-32delinsGT
XM_006722004.3:c.615-30_615-29delinsGT XP_006722067.1:n.615-30_615-29delinsGT
XM_006722005.3:c.615-30_615-29delinsGT XP_006722068.1:n.615-30_615-29delinsGT
XM_011525092.2:c.615-30_615-29delinsGT XP_011523394.1:n.615-30_615-29delinsGT
XM_011525093.2:c.615-30_615-29delinsGT XP_011523395.1:n.615-30_615-29delinsGT
XM_011525094.2:c.615-30_615-29delinsGT XP_011523396.1:n.615-30_615-29delinsGT
XM_017024914.1:c.615-33_615-32delinsGT XP_016880403.1:n.615-33_615-32delinsGT
XM_017024915.1:c.615-33_615-32delinsGT XP_016880404.1:n.615-33_615-32delinsGT
XM_017024916.1:c.615-33_615-32delinsGT XP_016880405.1:n.615-33_615-32delinsGT
XM_017024917.1:c.615-33_615-32delinsGT XP_016880406.1:n.615-33_615-32delinsGT
XM_017024918.2:c.615-33_615-32delinsGT XP_016880407.1:n.615-33_615-32delinsGT
XM_017024919.1:c.554-33_554-32delinsGT XP_016880408.1:n.554-33_554-32delinsGT
XR_934513.3:n.1615-33_1615-32delinsGT
XR_934514.3:n.1615-30_1615-29delinsGT
XR_934886.2:n.149+5619_149+5620delinsAC
NM_058216.3:c.966-33_966-32delinsGT MANE Select NP_478123.1:n.966-33_966-32delinsGT
NR_103872.2:n.841-33_841-32delinsGT