Canonical Allele Identifier: CA2267813931
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692608A= , CM000679.2:g.58692608A= GRCh38
NC_000017.10:g.56769969A= , CM000679.1:g.56769969A= GRCh37
NC_000017.9:g.54124968A= NCBI36
NG_023199.1:g.5007A= , LRG_314:g.5007A=
NG_047169.1:g.4472T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-284A= ENSP00000464056.2:n.-284A=
ENST00000697675.1:n.36A=
ENST00000697676.1:n.25A=
ENST00000697677.1:n.23A=
ENST00000697678.1:n.23A=
ENST00000697679.1:n.16A=
ENST00000697680.1:c.-36A= ENSP00000513392.1:n.-36A=
ENST00000697681.1:c.-36A= ENSP00000513393.1:n.-36A=
ENST00000697683.1:c.-36A= ENSP00000513395.1:n.-36A=
ENST00000697684.1:n.25A=
ENST00000697685.1:c.-36A= ENSP00000513396.1:n.-36A=
ENST00000697686.1:c.-231A= ENSP00000513397.1:n.-231A=
ENST00000697687.1:n.11A=
ENST00000697688.1:n.11A=
ENST00000697689.1:c.-36A= ENSP00000513398.1:n.-36A=
ENST00000697690.1:c.-36A= ENSP00000513399.1:n.-36A=
ENST00000337432.9:c.-36A= MANE Select ENSP00000336701.4:n.-36A=
ENST00000337432.8:c.-36A= ENSP00000336701.4:n.-36A=
ENST00000461271.5:c.-284A= ENSP00000464056.1:n.-284A=
ENST00000475762.5:c.-36A= ENSP00000432421.1:n.-36A=
ENST00000476741.2:n.7A=
ENST00000486827.1:c.-36A= ENSP00000436761.1:n.-36A=
ENST00000487525.5:c.-36A= ENSP00000431637.1:n.-36A=
ENST00000487921.5:n.33A=
ENST00000583539.5:c.-36A= ENSP00000463121.1:n.-36A=
NM_002876.3:c.-36A= NP_002867.1:n.-36A=
NM_058216.2:c.-36A= NP_478123.1:n.-36A=
NR_103872.1:n.36A=
NR_103873.1:n.36A=
XM_006722001.2:c.-36A= XP_006722064.1:n.-36A=
XM_006722002.2:c.-36A= XP_006722065.1:n.-36A=
XM_006722004.2:c.-284A= XP_006722067.1:n.-284A=
XM_006722005.2:c.-231A= XP_006722068.1:n.-231A=
XM_011525092.1:c.-584A= XP_011523394.1:n.-584A=
XM_011525093.1:c.-745A= XP_011523395.1:n.-745A=
XR_934513.1:n.38A=
XR_934514.1:n.38A=
XM_006722001.4:c.-36A= XP_006722064.1:n.-36A=
XM_006722002.4:c.-36A= XP_006722065.1:n.-36A=
XM_006722004.3:c.-284A= XP_006722067.1:n.-284A=
XM_006722005.3:c.-231A= XP_006722068.1:n.-231A=
XM_017024914.1:c.-284A= XP_016880403.1:n.-284A=
XM_017024917.1:c.-231A= XP_016880406.1:n.-231A=
XR_934513.3:n.469A=
XR_934514.3:n.469A=
NM_058216.3:c.-36A= MANE Select NP_478123.1:n.-36A=
NR_103872.2:n.7A=
NM_002876.4:c.-36A= NP_002867.1:n.-36A=