Canonical Allele Identifier: CA2267813905
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692579A= , CM000679.2:g.58692579A= GRCh38
NC_000017.10:g.56769940A= , CM000679.1:g.56769940A= GRCh37
NC_000017.9:g.54124939A= NCBI36
NG_023199.1:g.4978A= , LRG_314:g.4978A=
NG_047169.1:g.4501T=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-313A= ENSP00000464056.2:n.-313A=
ENST00000697675.1:n.7A=
ENST00000697683.1:c.-65A= ENSP00000513395.1:n.-65A=
ENST00000337432.8:c.-65A= ENSP00000336701.4:n.-65A=
ENST00000461271.5:c.-313A= ENSP00000464056.1:n.-313A=
ENST00000487921.5:n.4A=
ENST00000583539.5:c.-65A= ENSP00000463121.1:n.-65A=
NM_002876.3:c.-65A= NP_002867.1:n.-65A=
NM_058216.2:c.-65A= NP_478123.1:n.-65A=
NR_103872.1:n.7A=
NR_103873.1:n.7A=
XM_006722001.2:c.-65A= XP_006722064.1:n.-65A=
XM_006722002.2:c.-65A= XP_006722065.1:n.-65A=
XM_006722004.2:c.-313A= XP_006722067.1:n.-313A=
XM_006722005.2:c.-260A= XP_006722068.1:n.-260A=
XR_934513.1:n.9A=
XR_934514.1:n.9A=
XM_006722001.4:c.-65A= XP_006722064.1:n.-65A=
XM_006722002.4:c.-65A= XP_006722065.1:n.-65A=
XM_006722004.3:c.-313A= XP_006722067.1:n.-313A=
XM_006722005.3:c.-260A= XP_006722068.1:n.-260A=
XM_017024914.1:c.-313A= XP_016880403.1:n.-313A=
XM_017024917.1:c.-260A= XP_016880406.1:n.-260A=
XR_934513.3:n.440A=
XR_934514.3:n.440A=