Canonical Allele Identifier: CA2639016855
Gene: RAD51C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724016dup , CM000679.2:g.58724016dup GRCh38
NC_000017.10:g.56801377dup , CM000679.1:g.56801377dup GRCh37
NC_000017.9:g.54156376dup NCBI36
NG_023199.1:g.36415dup , LRG_314:g.36415dup

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.554-24dup ENSP00000464056.2:n.554-24dup
ENST00000697680.1:c.*1869-24dup ENSP00000513392.1:n.*1869-24dup
ENST00000697681.1:c.*2066-24dup ENSP00000513393.1:n.*2066-24dup
ENST00000697683.1:c.*1769-24dup ENSP00000513395.1:n.*1769-24dup
ENST00000697684.1:n.965-24dup
ENST00000697685.1:c.*1602-24dup ENSP00000513396.1:n.*1602-24dup
ENST00000697686.1:c.554-24dup ENSP00000513397.1:n.554-24dup
ENST00000697687.1:n.784-24dup
ENST00000697688.1:n.951-24dup
ENST00000697689.1:c.*1440+3204dup ENSP00000513398.1:n.*1440+3204dup
ENST00000697690.1:c.904+3204dup ENSP00000513399.1:n.904+3204dup
ENST00000697691.1:c.*877-24dup ENSP00000513400.1:n.*877-24dup
ENST00000697692.1:c.*917-24dup ENSP00000513401.1:n.*917-24dup
ENST00000697694.1:c.554-24dup ENSP00000513402.1:n.554-24dup
ENST00000697695.1:n.1512-24dup
ENST00000337432.9:c.905-24dup MANE Select ENSP00000336701.4:n.905-24dup
ENST00000337432.8:c.905-24dup ENSP00000336701.4:n.905-24dup
ENST00000413590.5:c.543-24dup
ENST00000475762.5:c.*1541-24dup ENSP00000432421.1:n.*1541-24dup
ENST00000482007.5:c.*333-24dup ENSP00000433332.1:n.*333-24dup
ENST00000487525.5:c.*478-24dup ENSP00000431637.1:n.*478-24dup
ENST00000578151.1:n.239+3204dup
ENST00000581221.5:n.420-24dup
ENST00000583539.5:c.905-24dup ENSP00000463121.1:n.905-24dup
ENST00000584617.5:c.627-24dup
ENST00000584804.1:c.199+3204dup ENSP00000463658.1:n.199+3204dup
NM_058216.2:c.905-24dup NP_478123.1:n.905-24dup
NR_103872.1:n.809-24dup
XM_006722001.2:c.905-24dup XP_006722064.1:n.905-24dup
XM_006722002.2:c.904+3204dup XP_006722065.1:n.904+3204dup
XM_006722004.2:c.554-24dup XP_006722067.1:n.554-24dup
XM_006722005.2:c.554-24dup XP_006722068.1:n.554-24dup
XM_011525092.1:c.554-24dup XP_011523394.1:n.554-24dup
XM_011525093.1:c.554-24dup XP_011523395.1:n.554-24dup
XM_011525094.1:c.554-24dup XP_011523396.1:n.554-24dup
XR_934513.1:n.1123-24dup
XR_934514.1:n.1123-24dup
XM_006722001.4:c.905-24dup XP_006722064.1:n.905-24dup
XM_006722002.4:c.904+3204dup XP_006722065.1:n.904+3204dup
XM_006722004.3:c.554-24dup XP_006722067.1:n.554-24dup
XM_006722005.3:c.554-24dup XP_006722068.1:n.554-24dup
XM_011525092.2:c.554-24dup XP_011523394.1:n.554-24dup
XM_011525093.2:c.554-24dup XP_011523395.1:n.554-24dup
XM_011525094.2:c.554-24dup XP_011523396.1:n.554-24dup
XM_017024914.1:c.554-24dup XP_016880403.1:n.554-24dup
XM_017024915.1:c.554-24dup XP_016880404.1:n.554-24dup
XM_017024916.1:c.554-24dup XP_016880405.1:n.554-24dup
XM_017024917.1:c.554-24dup XP_016880406.1:n.554-24dup
XM_017024918.2:c.554-24dup XP_016880407.1:n.554-24dup
XM_017024919.1:c.553+3204dup XP_016880408.1:n.553+3204dup
XR_934513.3:n.1554-24dup
XR_934514.3:n.1554-24dup
NM_058216.3:c.905-24dup MANE Select NP_478123.1:n.905-24dup
NR_103872.2:n.780-24dup