Canonical Allele Identifier: CA2267813918
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692596G= , CM000679.2:g.58692596G= GRCh38
NC_000017.10:g.56769957G= , CM000679.1:g.56769957G= GRCh37
NC_000017.9:g.54124956G= NCBI36
NG_023199.1:g.4995G= , LRG_314:g.4995G=
NG_047169.1:g.4484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-296G= ENSP00000464056.2:n.-296G=
ENST00000697675.1:n.24G=
ENST00000697676.1:n.13G=
ENST00000697677.1:n.11G=
ENST00000697678.1:n.11G=
ENST00000697679.1:n.4G=
ENST00000697680.1:c.-48G= ENSP00000513392.1:n.-48G=
ENST00000697681.1:c.-48G= ENSP00000513393.1:n.-48G=
ENST00000697683.1:c.-48G= ENSP00000513395.1:n.-48G=
ENST00000697684.1:n.13G=
ENST00000697685.1:c.-48G= ENSP00000513396.1:n.-48G=
ENST00000697686.1:c.-243G= ENSP00000513397.1:n.-243G=
ENST00000337432.8:c.-48G= ENSP00000336701.4:n.-48G=
ENST00000461271.5:c.-296G= ENSP00000464056.1:n.-296G=
ENST00000487921.5:n.21G=
ENST00000583539.5:c.-48G= ENSP00000463121.1:n.-48G=
NM_002876.3:c.-48G= NP_002867.1:n.-48G=
NM_058216.2:c.-48G= NP_478123.1:n.-48G=
NR_103872.1:n.24G=
NR_103873.1:n.24G=
XM_006722001.2:c.-48G= XP_006722064.1:n.-48G=
XM_006722002.2:c.-48G= XP_006722065.1:n.-48G=
XM_006722004.2:c.-296G= XP_006722067.1:n.-296G=
XM_006722005.2:c.-243G= XP_006722068.1:n.-243G=
XM_011525092.1:c.-596G= XP_011523394.1:n.-596G=
XM_011525093.1:c.-757G= XP_011523395.1:n.-757G=
XR_934513.1:n.26G=
XR_934514.1:n.26G=
XM_006722001.4:c.-48G= XP_006722064.1:n.-48G=
XM_006722002.4:c.-48G= XP_006722065.1:n.-48G=
XM_006722004.3:c.-296G= XP_006722067.1:n.-296G=
XM_006722005.3:c.-243G= XP_006722068.1:n.-243G=
XM_017024914.1:c.-296G= XP_016880403.1:n.-296G=
XM_017024917.1:c.-243G= XP_016880406.1:n.-243G=
XR_934513.3:n.457G=
XR_934514.3:n.457G=