Canonical Allele Identifier: CA2267813925
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692602G= , CM000679.2:g.58692602G= GRCh38
NC_000017.10:g.56769963G= , CM000679.1:g.56769963G= GRCh37
NC_000017.9:g.54124962G= NCBI36
NG_023199.1:g.5001G= , LRG_314:g.5001G=
NG_047169.1:g.4478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461271.6:c.-290G= ENSP00000464056.2:n.-290G=
ENST00000697675.1:n.30G=
ENST00000697676.1:n.19G=
ENST00000697677.1:n.17G=
ENST00000697678.1:n.17G=
ENST00000697679.1:n.10G=
ENST00000697680.1:c.-42G= ENSP00000513392.1:n.-42G=
ENST00000697681.1:c.-42G= ENSP00000513393.1:n.-42G=
ENST00000697683.1:c.-42G= ENSP00000513395.1:n.-42G=
ENST00000697684.1:n.19G=
ENST00000697685.1:c.-42G= ENSP00000513396.1:n.-42G=
ENST00000697686.1:c.-237G= ENSP00000513397.1:n.-237G=
ENST00000697687.1:n.5G=
ENST00000697688.1:n.5G=
ENST00000697689.1:c.-42G= ENSP00000513398.1:n.-42G=
ENST00000697690.1:c.-42G= ENSP00000513399.1:n.-42G=
ENST00000337432.9:c.-42G= MANE Select ENSP00000336701.4:n.-42G=
ENST00000337432.8:c.-42G= ENSP00000336701.4:n.-42G=
ENST00000461271.5:c.-290G= ENSP00000464056.1:n.-290G=
ENST00000475762.5:c.-42G= ENSP00000432421.1:n.-42G=
ENST00000476741.2:n.1G=
ENST00000487921.5:n.27G=
ENST00000583539.5:c.-42G= ENSP00000463121.1:n.-42G=
NM_002876.3:c.-42G= NP_002867.1:n.-42G=
NM_058216.2:c.-42G= NP_478123.1:n.-42G=
NR_103872.1:n.30G=
NR_103873.1:n.30G=
XM_006722001.2:c.-42G= XP_006722064.1:n.-42G=
XM_006722002.2:c.-42G= XP_006722065.1:n.-42G=
XM_006722004.2:c.-290G= XP_006722067.1:n.-290G=
XM_006722005.2:c.-237G= XP_006722068.1:n.-237G=
XM_011525092.1:c.-590G= XP_011523394.1:n.-590G=
XM_011525093.1:c.-751G= XP_011523395.1:n.-751G=
XR_934513.1:n.32G=
XR_934514.1:n.32G=
XM_006722001.4:c.-42G= XP_006722064.1:n.-42G=
XM_006722002.4:c.-42G= XP_006722065.1:n.-42G=
XM_006722004.3:c.-290G= XP_006722067.1:n.-290G=
XM_006722005.3:c.-237G= XP_006722068.1:n.-237G=
XM_017024914.1:c.-290G= XP_016880403.1:n.-290G=
XM_017024917.1:c.-237G= XP_016880406.1:n.-237G=
XR_934513.3:n.463G=
XR_934514.3:n.463G=
NM_058216.3:c.-42G= MANE Select NP_478123.1:n.-42G=
NR_103872.2:n.1G=
NM_002876.4:c.-42G= NP_002867.1:n.-42G=