Canonical Allele Identifier: CA3261180113
Community Standard Title: NM_058216.3(RAD51C):c.104_105delinsTG (p.Ala35Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692747_58692748delinsTG , CM000679.2:g.58692747_58692748delinsTG GRCh38
NC_000017.10:g.56770108_56770109delinsTG , CM000679.1:g.56770108_56770109delinsTG GRCh37
NC_000017.9:g.54125107_54125108delinsTG NCBI36
NG_023199.1:g.5146_5147delinsTG , LRG_314:g.5146_5147delinsTG
NG_047169.1:g.4332_4333delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.104_105delinsTG MANE Select NP_478123.1:p.Ala35Val
ENST00000337432.9:c.104_105delinsTG MANE Select ENSP00000336701.4:p.Ala35Val
NM_002876.3:c.104_105delinsTG NP_002867.1:p.Ala35Val
NM_002876.4:c.104_105delinsTG NP_002867.1:p.Ala35Val
NM_058216.2:c.104_105delinsTG NP_478123.1:p.Ala35Val
NR_103872.1:n.175_176delinsTG
NR_103872.2:n.146_147delinsTG
NR_103873.1:n.113+62_113+63delinsTG
ENST00000337432.8:c.104_105delinsTG ENSP00000336701.4:p.Ala35Val
ENST00000421782.3:c.104_105delinsTG ENSP00000391450.2:p.Ala35Val
ENST00000461271.5:c.-207+62_-207+63delinsTG ENSP00000464056.1:n.-207+62_-207+63delinsTG
ENST00000461271.6:c.-207+62_-207+63delinsTG ENSP00000464056.2:n.-207+62_-207+63delinsTG
ENST00000475762.5:c.104_105delinsTG ENSP00000432421.1:p.Ala35Val
ENST00000476741.2:n.146_147delinsTG
ENST00000482007.5:c.104_105delinsTG ENSP00000433332.1:p.Ala35Val
ENST00000486827.1:c.104_105delinsTG ENSP00000436761.1:p.Ala35Val
ENST00000487525.5:c.104_105delinsTG ENSP00000431637.1:p.Ala35Val
ENST00000487921.5:n.57+115_57+116delinsTG
ENST00000583539.5:c.104_105delinsTG ENSP00000463121.1:p.Ala35Val
ENST00000584617.5:c.85_86delinsTG
ENST00000697675.1:n.175_176delinsTG
ENST00000697676.1:n.164_165delinsTG
ENST00000697677.1:n.162_163delinsTG
ENST00000697678.1:n.47+115_47+116delinsTG
ENST00000697679.1:n.155_156delinsTG
ENST00000697680.1:c.104_105delinsTG ENSP00000513392.1:p.Ala35Val
ENST00000697681.1:c.104_105delinsTG ENSP00000513393.1:p.Ala35Val
ENST00000697683.1:c.104_105delinsTG ENSP00000513395.1:p.Ala35Val
ENST00000697684.1:n.164_165delinsTG
ENST00000697685.1:c.104_105delinsTG ENSP00000513396.1:p.Ala35Val
ENST00000697686.1:c.-207+115_-207+116delinsTG ENSP00000513397.1:n.-207+115_-207+116delinsTG
ENST00000697687.1:n.150_151delinsTG
ENST00000697688.1:n.150_151delinsTG
ENST00000697689.1:c.104_105delinsTG ENSP00000513398.1:p.Ala35Val
ENST00000697690.1:c.104_105delinsTG ENSP00000513399.1:p.Ala35Val
ENST00000697691.1:c.42+62_42+63delinsTG ENSP00000513400.1:n.42+62_42+63delinsTG
ENST00000697692.1:c.104_105delinsTG ENSP00000513401.1:p.Ala35Val
ENST00000697693.1:n.17_18delinsTG
XM_006722001.2:c.104_105delinsTG XP_006722064.1:p.Ala35Val
XM_006722001.4:c.104_105delinsTG XP_006722064.1:p.Ala35Val
XM_006722002.2:c.104_105delinsTG XP_006722065.1:p.Ala35Val
XM_006722002.4:c.104_105delinsTG XP_006722065.1:p.Ala35Val
XM_006722004.2:c.-207+62_-207+63delinsTG XP_006722067.1:n.-207+62_-207+63delinsTG
XM_006722004.3:c.-207+62_-207+63delinsTG XP_006722067.1:n.-207+62_-207+63delinsTG
XM_006722005.2:c.-207+115_-207+116delinsTG XP_006722068.1:n.-207+115_-207+116delinsTG
XM_006722005.3:c.-207+115_-207+116delinsTG XP_006722068.1:n.-207+115_-207+116delinsTG
XM_011525092.1:c.-507+62_-507+63delinsTG XP_011523394.1:n.-507+62_-507+63delinsTG
XM_011525092.2:c.-507+62_-507+63delinsTG XP_011523394.1:n.-507+62_-507+63delinsTG
XM_011525093.1:c.-668+62_-668+63delinsTG XP_011523395.1:n.-668+62_-668+63delinsTG
XM_011525093.2:c.-668+62_-668+63delinsTG XP_011523395.1:n.-668+62_-668+63delinsTG
XM_017024914.1:c.-207+62_-207+63delinsTG XP_016880403.1:n.-207+62_-207+63delinsTG
XM_017024916.1:c.-507+62_-507+63delinsTG XP_016880405.1:n.-507+62_-507+63delinsTG
XM_017024917.1:c.-207+115_-207+116delinsTG XP_016880406.1:n.-207+115_-207+116delinsTG
XM_017024918.2:c.-419_-418delinsTG XP_016880407.1:n.-419_-418delinsTG
XM_017024919.1:c.-668+62_-668+63delinsTG XP_016880408.1:n.-668+62_-668+63delinsTG
XR_934513.1:n.177_178delinsTG
XR_934513.3:n.608_609delinsTG
XR_934514.1:n.177_178delinsTG
XR_934514.3:n.608_609delinsTG