Canonical Allele Identifier: CA2267833208
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732481C= , CM000679.2:g.58732481C= GRCh38
NC_000017.10:g.56809842C= , CM000679.1:g.56809842C= GRCh37
NC_000017.9:g.54164841C= NCBI36
NG_023199.1:g.44880C= , LRG_314:g.44880C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.615-3C= ENSP00000464056.2:n.615-3C=
ENST00000697680.1:c.*1930-3C= ENSP00000513392.1:n.*1930-3C=
ENST00000697681.1:c.*2127-3C= ENSP00000513393.1:n.*2127-3C=
ENST00000697683.1:c.*1902-3C= ENSP00000513395.1:n.*1902-3C=
ENST00000697685.1:c.*1663-3C= ENSP00000513396.1:n.*1663-3C=
ENST00000697686.1:c.737-3C= ENSP00000513397.1:n.737-3C=
ENST00000697689.1:c.*1441-1637C= ENSP00000513398.1:n.*1441-1637C=
ENST00000697690.1:c.905-1637C= ENSP00000513399.1:n.905-1637C=
ENST00000697691.1:c.*938-3C= ENSP00000513400.1:n.*938-3C=
ENST00000697692.1:c.*978-3C= ENSP00000513401.1:n.*978-3C=
ENST00000697694.1:c.615-3C= ENSP00000513402.1:n.615-3C=
ENST00000697695.1:n.1573-3C=
ENST00000337432.9:c.966-3C= MANE Select ENSP00000336701.4:n.966-3C=
ENST00000337432.8:c.966-3C= ENSP00000336701.4:n.966-3C=
ENST00000413590.5:c.604C=
ENST00000461706.1:n.150C=
ENST00000475762.5:c.*1602-3C= ENSP00000432421.1:n.*1602-3C=
ENST00000482007.5:c.*394-3C= ENSP00000433332.1:n.*394-3C=
ENST00000487525.5:c.*539C= ENSP00000431637.1:n.*539C=
ENST00000578151.1:n.240-1637C=
ENST00000581221.5:n.481-3C=
ENST00000583539.5:c.966-3C= ENSP00000463121.1:n.966-3C=
ENST00000584617.5:c.688-3C=
ENST00000584804.1:c.200-3C= ENSP00000463658.1:n.200-3C=
NM_058216.2:c.966-3C= NP_478123.1:n.966-3C=
NR_103872.1:n.870-3C=
XM_006722001.2:c.966C= XP_006722064.1:p.Ser322=
XM_006722002.2:c.905-3C= XP_006722065.1:n.905-3C=
XM_006722004.2:c.615C= XP_006722067.1:p.Ser205=
XM_006722005.2:c.615C= XP_006722068.1:p.Ser205=
XM_011525092.1:c.615C= XP_011523394.1:p.Ser205=
XM_011525093.1:c.615C= XP_011523395.1:p.Ser205=
XM_011525094.1:c.615C= XP_011523396.1:p.Ser205=
XR_934513.1:n.1184-3C=
XR_934514.1:n.1184C=
XR_934886.1:n.149+5590G=
XM_006722001.4:c.966C= XP_006722064.1:p.Ser322=
XM_006722002.4:c.905-3C= XP_006722065.1:n.905-3C=
XM_006722004.3:c.615C= XP_006722067.1:p.Ser205=
XM_006722005.3:c.615C= XP_006722068.1:p.Ser205=
XM_011525092.2:c.615C= XP_011523394.1:p.Ser205=
XM_011525093.2:c.615C= XP_011523395.1:p.Ser205=
XM_011525094.2:c.615C= XP_011523396.1:p.Ser205=
XM_017024914.1:c.615-3C= XP_016880403.1:n.615-3C=
XM_017024915.1:c.615-3C= XP_016880404.1:n.615-3C=
XM_017024916.1:c.615-3C= XP_016880405.1:n.615-3C=
XM_017024917.1:c.615-3C= XP_016880406.1:n.615-3C=
XM_017024918.2:c.615-3C= XP_016880407.1:n.615-3C=
XM_017024919.1:c.554-3C= XP_016880408.1:n.554-3C=
XR_934513.3:n.1615-3C=
XR_934514.3:n.1615C=
XR_934886.2:n.149+5590G=
NM_058216.3:c.966-3C= MANE Select NP_478123.1:n.966-3C=
NR_103872.2:n.841-3C=