Canonical Allele Identifier: CA3261180519
Community Standard Title: NM_058216.3(RAD51C):c.134_135delinsCC (p.Glu45Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692777_58692778delinsCC , CM000679.2:g.58692777_58692778delinsCC GRCh38
NC_000017.10:g.56770138_56770139delinsCC , CM000679.1:g.56770138_56770139delinsCC GRCh37
NC_000017.9:g.54125137_54125138delinsCC NCBI36
NG_023199.1:g.5176_5177delinsCC , LRG_314:g.5176_5177delinsCC
NG_047169.1:g.4302_4303delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.134_135delinsCC MANE Select NP_478123.1:p.Glu45Ala
ENST00000337432.9:c.134_135delinsCC MANE Select ENSP00000336701.4:p.Glu45Ala
NM_002876.3:c.134_135delinsCC NP_002867.1:p.Glu45Ala
NM_002876.4:c.134_135delinsCC NP_002867.1:p.Glu45Ala
NM_058216.2:c.134_135delinsCC NP_478123.1:p.Glu45Ala
NR_103872.1:n.205_206delinsCC
NR_103872.2:n.176_177delinsCC
NR_103873.1:n.113+92_113+93delinsCC
ENST00000337432.8:c.134_135delinsCC ENSP00000336701.4:p.Glu45Ala
ENST00000421782.3:c.134_135delinsCC ENSP00000391450.2:p.Glu45Ala
ENST00000461271.5:c.-207+92_-207+93delinsCC ENSP00000464056.1:n.-207+92_-207+93delinsCC
ENST00000461271.6:c.-207+92_-207+93delinsCC ENSP00000464056.2:n.-207+92_-207+93delinsCC
ENST00000475762.5:c.134_135delinsCC ENSP00000432421.1:p.Glu45Ala
ENST00000476741.2:n.176_177delinsCC
ENST00000482007.5:c.134_135delinsCC ENSP00000433332.1:p.Glu45Ala
ENST00000486827.1:c.134_135delinsCC ENSP00000436761.1:p.Glu45Ala
ENST00000487525.5:c.134_135delinsCC ENSP00000431637.1:p.Glu45Ala
ENST00000487921.5:n.57+145_57+146delinsCC
ENST00000583539.5:c.134_135delinsCC ENSP00000463121.1:p.Glu45Ala
ENST00000584617.5:c.115_116delinsCC
ENST00000697675.1:n.205_206delinsCC
ENST00000697676.1:n.194_195delinsCC
ENST00000697677.1:n.192_193delinsCC
ENST00000697678.1:n.47+145_47+146delinsCC
ENST00000697679.1:n.185_186delinsCC
ENST00000697680.1:c.134_135delinsCC ENSP00000513392.1:p.Glu45Ala
ENST00000697681.1:c.134_135delinsCC ENSP00000513393.1:p.Glu45Ala
ENST00000697683.1:c.134_135delinsCC ENSP00000513395.1:p.Glu45Ala
ENST00000697684.1:n.194_195delinsCC
ENST00000697685.1:c.134_135delinsCC ENSP00000513396.1:p.Glu45Ala
ENST00000697686.1:c.-207+145_-207+146delinsCC ENSP00000513397.1:n.-207+145_-207+146delinsCC
ENST00000697687.1:n.180_181delinsCC
ENST00000697688.1:n.180_181delinsCC
ENST00000697689.1:c.134_135delinsCC ENSP00000513398.1:p.Glu45Ala
ENST00000697690.1:c.134_135delinsCC ENSP00000513399.1:p.Glu45Ala
ENST00000697691.1:c.42+92_42+93delinsCC ENSP00000513400.1:n.42+92_42+93delinsCC
ENST00000697692.1:c.134_135delinsCC ENSP00000513401.1:p.Glu45Ala
ENST00000697693.1:n.47_48delinsCC
XM_006722001.2:c.134_135delinsCC XP_006722064.1:p.Glu45Ala
XM_006722001.4:c.134_135delinsCC XP_006722064.1:p.Glu45Ala
XM_006722002.2:c.134_135delinsCC XP_006722065.1:p.Glu45Ala
XM_006722002.4:c.134_135delinsCC XP_006722065.1:p.Glu45Ala
XM_006722004.2:c.-207+92_-207+93delinsCC XP_006722067.1:n.-207+92_-207+93delinsCC
XM_006722004.3:c.-207+92_-207+93delinsCC XP_006722067.1:n.-207+92_-207+93delinsCC
XM_006722005.2:c.-207+145_-207+146delinsCC XP_006722068.1:n.-207+145_-207+146delinsCC
XM_006722005.3:c.-207+145_-207+146delinsCC XP_006722068.1:n.-207+145_-207+146delinsCC
XM_011525092.1:c.-507+92_-507+93delinsCC XP_011523394.1:n.-507+92_-507+93delinsCC
XM_011525092.2:c.-507+92_-507+93delinsCC XP_011523394.1:n.-507+92_-507+93delinsCC
XM_011525093.1:c.-668+92_-668+93delinsCC XP_011523395.1:n.-668+92_-668+93delinsCC
XM_011525093.2:c.-668+92_-668+93delinsCC XP_011523395.1:n.-668+92_-668+93delinsCC
XM_017024914.1:c.-207+92_-207+93delinsCC XP_016880403.1:n.-207+92_-207+93delinsCC
XM_017024916.1:c.-507+92_-507+93delinsCC XP_016880405.1:n.-507+92_-507+93delinsCC
XM_017024917.1:c.-207+145_-207+146delinsCC XP_016880406.1:n.-207+145_-207+146delinsCC
XM_017024918.2:c.-389_-388delinsCC XP_016880407.1:n.-389_-388delinsCC
XM_017024919.1:c.-668+92_-668+93delinsCC XP_016880408.1:n.-668+92_-668+93delinsCC
XR_934513.1:n.207_208delinsCC
XR_934513.3:n.638_639delinsCC
XR_934514.1:n.207_208delinsCC
XR_934514.3:n.638_639delinsCC