Canonical Allele Identifier: CA2267813948
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692619T= , CM000679.2:g.58692619T= GRCh38
NC_000017.10:g.56769980T= , CM000679.1:g.56769980T= GRCh37
NC_000017.9:g.54124979T= NCBI36
NG_023199.1:g.5018T= , LRG_314:g.5018T=
NG_047169.1:g.4461A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-273T= ENSP00000464056.2:n.-273T=
ENST00000697675.1:n.47T=
ENST00000697676.1:n.36T=
ENST00000697677.1:n.34T=
ENST00000697678.1:n.34T=
ENST00000697679.1:n.27T=
ENST00000697680.1:c.-25T= ENSP00000513392.1:n.-25T=
ENST00000697681.1:c.-25T= ENSP00000513393.1:n.-25T=
ENST00000697683.1:c.-25T= ENSP00000513395.1:n.-25T=
ENST00000697684.1:n.36T=
ENST00000697685.1:c.-25T= ENSP00000513396.1:n.-25T=
ENST00000697686.1:c.-220T= ENSP00000513397.1:n.-220T=
ENST00000697687.1:n.22T=
ENST00000697688.1:n.22T=
ENST00000697689.1:c.-25T= ENSP00000513398.1:n.-25T=
ENST00000697690.1:c.-25T= ENSP00000513399.1:n.-25T=
ENST00000697691.1:c.-25T= ENSP00000513400.1:n.-25T=
ENST00000337432.9:c.-25T= MANE Select ENSP00000336701.4:n.-25T=
ENST00000337432.8:c.-25T= ENSP00000336701.4:n.-25T=
ENST00000461271.5:c.-273T= ENSP00000464056.1:n.-273T=
ENST00000475762.5:c.-25T= ENSP00000432421.1:n.-25T=
ENST00000476741.2:n.18T=
ENST00000482007.5:c.-25T= ENSP00000433332.1:n.-25T=
ENST00000486827.1:c.-25T= ENSP00000436761.1:n.-25T=
ENST00000487525.5:c.-25T= ENSP00000431637.1:n.-25T=
ENST00000487921.5:n.44T=
ENST00000583539.5:c.-25T= ENSP00000463121.1:n.-25T=
NM_002876.3:c.-25T= NP_002867.1:n.-25T=
NM_058216.2:c.-25T= NP_478123.1:n.-25T=
NR_103872.1:n.47T=
NR_103873.1:n.47T=
XM_006722001.2:c.-25T= XP_006722064.1:n.-25T=
XM_006722002.2:c.-25T= XP_006722065.1:n.-25T=
XM_006722004.2:c.-273T= XP_006722067.1:n.-273T=
XM_006722005.2:c.-220T= XP_006722068.1:n.-220T=
XM_011525092.1:c.-573T= XP_011523394.1:n.-573T=
XM_011525093.1:c.-734T= XP_011523395.1:n.-734T=
XR_934513.1:n.49T=
XR_934514.1:n.49T=
XM_006722001.4:c.-25T= XP_006722064.1:n.-25T=
XM_006722002.4:c.-25T= XP_006722065.1:n.-25T=
XM_006722004.3:c.-273T= XP_006722067.1:n.-273T=
XM_006722005.3:c.-220T= XP_006722068.1:n.-220T=
XM_017024914.1:c.-273T= XP_016880403.1:n.-273T=
XM_017024916.1:c.-573T= XP_016880405.1:n.-573T=
XM_017024917.1:c.-220T= XP_016880406.1:n.-220T=
XR_934513.3:n.480T=
XR_934514.3:n.480T=
NM_058216.3:c.-25T= MANE Select NP_478123.1:n.-25T=
NR_103872.2:n.18T=
NM_002876.4:c.-25T= NP_002867.1:n.-25T=