Canonical Allele Identifier: CA2267814051
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692732_58692733delinsCG , CM000679.2:g.58692732_58692733delinsCG GRCh38
NC_000017.10:g.56770093_56770094delinsCG , CM000679.1:g.56770093_56770094delinsCG GRCh37
NC_000017.9:g.54125092_54125093delinsCG NCBI36
NG_023199.1:g.5131_5132delinsCG , LRG_314:g.5131_5132delinsCG
NG_047169.1:g.4347_4348delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-207+47_-207+48delinsCG ENSP00000464056.2:n.-207+47_-207+48delins...
ENST00000697675.1:n.160_161delinsCG
ENST00000697676.1:n.149_150delinsCG
ENST00000697677.1:n.147_148delinsCG
ENST00000697678.1:n.47+100_47+101delinsCG
ENST00000697679.1:n.140_141delinsCG
ENST00000697680.1:c.89_90delinsCG ENSP00000513392.1:p.Ala30=
ENST00000697681.1:c.89_90delinsCG ENSP00000513393.1:p.Ala30=
ENST00000697683.1:c.89_90delinsCG ENSP00000513395.1:p.Ala30=
ENST00000697684.1:n.149_150delinsCG
ENST00000697685.1:c.89_90delinsCG ENSP00000513396.1:p.Ala30=
ENST00000697686.1:c.-207+100_-207+101delinsCG ENSP00000513397.1:n.-207+100_-207+101deli...
ENST00000697687.1:n.135_136delinsCG
ENST00000697688.1:n.135_136delinsCG
ENST00000697689.1:c.89_90delinsCG ENSP00000513398.1:p.Ala30=
ENST00000697690.1:c.89_90delinsCG ENSP00000513399.1:p.Ala30=
ENST00000697691.1:c.42+47_42+48delinsCG ENSP00000513400.1:n.42+47_42+48delinsCG
ENST00000697692.1:c.89_90delinsCG ENSP00000513401.1:p.Ala30=
ENST00000697693.1:n.2_3delinsCG
ENST00000337432.9:c.89_90delinsCG MANE Select ENSP00000336701.4:p.Ala30=
ENST00000337432.8:c.89_90delinsCG ENSP00000336701.4:p.Ala30=
ENST00000421782.3:c.89_90delinsCG ENSP00000391450.2:p.Ala30=
ENST00000461271.5:c.-207+47_-207+48delinsCG ENSP00000464056.1:n.-207+47_-207+48delins...
ENST00000475762.5:c.89_90delinsCG ENSP00000432421.1:p.Ala30=
ENST00000476741.2:n.131_132delinsCG
ENST00000482007.5:c.89_90delinsCG ENSP00000433332.1:p.Ala30=
ENST00000486827.1:c.89_90delinsCG ENSP00000436761.1:p.Ala30=
ENST00000487525.5:c.89_90delinsCG ENSP00000431637.1:p.Ala30=
ENST00000487921.5:n.57+100_57+101delinsCG
ENST00000583539.5:c.89_90delinsCG ENSP00000463121.1:p.Ala30=
ENST00000584617.5:c.70_71delinsCG
NM_002876.3:c.89_90delinsCG NP_002867.1:p.Ala30=
NM_058216.2:c.89_90delinsCG NP_478123.1:p.Ala30=
NR_103872.1:n.160_161delinsCG
NR_103873.1:n.113+47_113+48delinsCG
XM_006722001.2:c.89_90delinsCG XP_006722064.1:p.Ala30=
XM_006722002.2:c.89_90delinsCG XP_006722065.1:p.Ala30=
XM_006722004.2:c.-207+47_-207+48delinsCG XP_006722067.1:n.-207+47_-207+48delinsCG
XM_006722005.2:c.-207+100_-207+101delinsCG XP_006722068.1:n.-207+100_-207+101delinsC...
XM_011525092.1:c.-507+47_-507+48delinsCG XP_011523394.1:n.-507+47_-507+48delinsCG
XM_011525093.1:c.-668+47_-668+48delinsCG XP_011523395.1:n.-668+47_-668+48delinsCG
XR_934513.1:n.162_163delinsCG
XR_934514.1:n.162_163delinsCG
XM_006722001.4:c.89_90delinsCG XP_006722064.1:p.Ala30=
XM_006722002.4:c.89_90delinsCG XP_006722065.1:p.Ala30=
XM_006722004.3:c.-207+47_-207+48delinsCG XP_006722067.1:n.-207+47_-207+48delinsCG
XM_006722005.3:c.-207+100_-207+101delinsCG XP_006722068.1:n.-207+100_-207+101delinsC...
XM_011525092.2:c.-507+47_-507+48delinsCG XP_011523394.1:n.-507+47_-507+48delinsCG
XM_011525093.2:c.-668+47_-668+48delinsCG XP_011523395.1:n.-668+47_-668+48delinsCG
XM_017024914.1:c.-207+47_-207+48delinsCG XP_016880403.1:n.-207+47_-207+48delinsCG
XM_017024916.1:c.-507+47_-507+48delinsCG XP_016880405.1:n.-507+47_-507+48delinsCG
XM_017024917.1:c.-207+100_-207+101delinsCG XP_016880406.1:n.-207+100_-207+101delinsC...
XM_017024918.2:c.-434_-433delinsCG XP_016880407.1:n.-434_-433delinsCG
XM_017024919.1:c.-668+47_-668+48delinsCG XP_016880408.1:n.-668+47_-668+48delinsCG
XR_934513.3:n.593_594delinsCG
XR_934514.3:n.593_594delinsCG
NM_058216.3:c.89_90delinsCG MANE Select NP_478123.1:p.Ala30=
NR_103872.2:n.131_132delinsCG
NM_002876.4:c.89_90delinsCG NP_002867.1:p.Ala30=