Canonical Allele Identifier: CA2267813966
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692637G= , CM000679.2:g.58692637G= GRCh38
NC_000017.10:g.56769998G= , CM000679.1:g.56769998G= GRCh37
NC_000017.9:g.54124997G= NCBI36
NG_023199.1:g.5036G= , LRG_314:g.5036G=
NG_047169.1:g.4443C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-255G= ENSP00000464056.2:n.-255G=
ENST00000697675.1:n.65G=
ENST00000697676.1:n.54G=
ENST00000697677.1:n.52G=
ENST00000697678.1:n.47+5G=
ENST00000697679.1:n.45G=
ENST00000697680.1:c.-7G= ENSP00000513392.1:n.-7G=
ENST00000697681.1:c.-7G= ENSP00000513393.1:n.-7G=
ENST00000697683.1:c.-7G= ENSP00000513395.1:n.-7G=
ENST00000697684.1:n.54G=
ENST00000697685.1:c.-7G= ENSP00000513396.1:n.-7G=
ENST00000697686.1:c.-207+5G= ENSP00000513397.1:n.-207+5G=
ENST00000697687.1:n.40G=
ENST00000697688.1:n.40G=
ENST00000697689.1:c.-7G= ENSP00000513398.1:n.-7G=
ENST00000697690.1:c.-7G= ENSP00000513399.1:n.-7G=
ENST00000697691.1:c.-7G= ENSP00000513400.1:n.-7G=
ENST00000697692.1:c.-7G= ENSP00000513401.1:n.-7G=
ENST00000337432.9:c.-7G= MANE Select ENSP00000336701.4:n.-7G=
ENST00000337432.8:c.-7G= ENSP00000336701.4:n.-7G=
ENST00000421782.3:c.-7G= ENSP00000391450.2:n.-7G=
ENST00000461271.5:c.-255G= ENSP00000464056.1:n.-255G=
ENST00000475762.5:c.-7G= ENSP00000432421.1:n.-7G=
ENST00000476741.2:n.36G=
ENST00000482007.5:c.-7G= ENSP00000433332.1:n.-7G=
ENST00000486827.1:c.-7G= ENSP00000436761.1:n.-7G=
ENST00000487525.5:c.-7G= ENSP00000431637.1:n.-7G=
ENST00000487921.5:n.57+5G=
ENST00000583539.5:c.-7G= ENSP00000463121.1:n.-7G=
NM_002876.3:c.-7G= NP_002867.1:n.-7G=
NM_058216.2:c.-7G= NP_478123.1:n.-7G=
NR_103872.1:n.65G=
NR_103873.1:n.65G=
XM_006722001.2:c.-7G= XP_006722064.1:n.-7G=
XM_006722002.2:c.-7G= XP_006722065.1:n.-7G=
XM_006722004.2:c.-255G= XP_006722067.1:n.-255G=
XM_006722005.2:c.-207+5G= XP_006722068.1:n.-207+5G=
XM_011525092.1:c.-555G= XP_011523394.1:n.-555G=
XM_011525093.1:c.-716G= XP_011523395.1:n.-716G=
XR_934513.1:n.67G=
XR_934514.1:n.67G=
XM_006722001.4:c.-7G= XP_006722064.1:n.-7G=
XM_006722002.4:c.-7G= XP_006722065.1:n.-7G=
XM_006722004.3:c.-255G= XP_006722067.1:n.-255G=
XM_006722005.3:c.-207+5G= XP_006722068.1:n.-207+5G=
XM_017024914.1:c.-255G= XP_016880403.1:n.-255G=
XM_017024916.1:c.-555G= XP_016880405.1:n.-555G=
XM_017024917.1:c.-207+5G= XP_016880406.1:n.-207+5G=
XM_017024918.2:c.-529G= XP_016880407.1:n.-529G=
XR_934513.3:n.498G=
XR_934514.3:n.498G=
NM_058216.3:c.-7G= MANE Select NP_478123.1:n.-7G=
NR_103872.2:n.36G=
NM_002876.4:c.-7G= NP_002867.1:n.-7G=