Canonical Allele Identifier: CA2267813967
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692638C= , CM000679.2:g.58692638C= GRCh38
NC_000017.10:g.56769999C= , CM000679.1:g.56769999C= GRCh37
NC_000017.9:g.54124998C= NCBI36
NG_023199.1:g.5037C= , LRG_314:g.5037C=
NG_047169.1:g.4442G=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-254C= ENSP00000464056.2:n.-254C=
ENST00000697675.1:n.66C=
ENST00000697676.1:n.55C=
ENST00000697677.1:n.53C=
ENST00000697678.1:n.47+6C=
ENST00000697679.1:n.46C=
ENST00000697680.1:c.-6C= ENSP00000513392.1:n.-6C=
ENST00000697681.1:c.-6C= ENSP00000513393.1:n.-6C=
ENST00000697683.1:c.-6C= ENSP00000513395.1:n.-6C=
ENST00000697684.1:n.55C=
ENST00000697685.1:c.-6C= ENSP00000513396.1:n.-6C=
ENST00000697686.1:c.-207+6C= ENSP00000513397.1:n.-207+6C=
ENST00000697687.1:n.41C=
ENST00000697688.1:n.41C=
ENST00000697689.1:c.-6C= ENSP00000513398.1:n.-6C=
ENST00000697690.1:c.-6C= ENSP00000513399.1:n.-6C=
ENST00000697691.1:c.-6C= ENSP00000513400.1:n.-6C=
ENST00000697692.1:c.-6C= ENSP00000513401.1:n.-6C=
ENST00000337432.9:c.-6C= MANE Select ENSP00000336701.4:n.-6C=
ENST00000337432.8:c.-6C= ENSP00000336701.4:n.-6C=
ENST00000421782.3:c.-6C= ENSP00000391450.2:n.-6C=
ENST00000461271.5:c.-254C= ENSP00000464056.1:n.-254C=
ENST00000475762.5:c.-6C= ENSP00000432421.1:n.-6C=
ENST00000476741.2:n.37C=
ENST00000482007.5:c.-6C= ENSP00000433332.1:n.-6C=
ENST00000486827.1:c.-6C= ENSP00000436761.1:n.-6C=
ENST00000487525.5:c.-6C= ENSP00000431637.1:n.-6C=
ENST00000487921.5:n.57+6C=
ENST00000583539.5:c.-6C= ENSP00000463121.1:n.-6C=
NM_002876.3:c.-6C= NP_002867.1:n.-6C=
NM_058216.2:c.-6C= NP_478123.1:n.-6C=
NR_103872.1:n.66C=
NR_103873.1:n.66C=
XM_006722001.2:c.-6C= XP_006722064.1:n.-6C=
XM_006722002.2:c.-6C= XP_006722065.1:n.-6C=
XM_006722004.2:c.-254C= XP_006722067.1:n.-254C=
XM_006722005.2:c.-207+6C= XP_006722068.1:n.-207+6C=
XM_011525092.1:c.-554C= XP_011523394.1:n.-554C=
XM_011525093.1:c.-715C= XP_011523395.1:n.-715C=
XR_934513.1:n.68C=
XR_934514.1:n.68C=
XM_006722001.4:c.-6C= XP_006722064.1:n.-6C=
XM_006722002.4:c.-6C= XP_006722065.1:n.-6C=
XM_006722004.3:c.-254C= XP_006722067.1:n.-254C=
XM_006722005.3:c.-207+6C= XP_006722068.1:n.-207+6C=
XM_017024914.1:c.-254C= XP_016880403.1:n.-254C=
XM_017024916.1:c.-554C= XP_016880405.1:n.-554C=
XM_017024917.1:c.-207+6C= XP_016880406.1:n.-207+6C=
XM_017024918.2:c.-528C= XP_016880407.1:n.-528C=
XR_934513.3:n.499C=
XR_934514.3:n.499C=
NM_058216.3:c.-6C= MANE Select NP_478123.1:n.-6C=
NR_103872.2:n.37C=
NM_002876.4:c.-6C= NP_002867.1:n.-6C=