Canonical Allele Identifier: CA3261180200
Community Standard Title: NM_058216.3(RAD51C):c.110_111delinsTG (p.Glu37Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692753_58692754delinsTG , CM000679.2:g.58692753_58692754delinsTG GRCh38
NC_000017.10:g.56770114_56770115delinsTG , CM000679.1:g.56770114_56770115delinsTG GRCh37
NC_000017.9:g.54125113_54125114delinsTG NCBI36
NG_023199.1:g.5152_5153delinsTG , LRG_314:g.5152_5153delinsTG
NG_047169.1:g.4326_4327delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.110_111delinsTG MANE Select NP_478123.1:p.Glu37Val
ENST00000337432.9:c.110_111delinsTG MANE Select ENSP00000336701.4:p.Glu37Val
NM_002876.3:c.110_111delinsTG NP_002867.1:p.Glu37Val
NM_002876.4:c.110_111delinsTG NP_002867.1:p.Glu37Val
NM_058216.2:c.110_111delinsTG NP_478123.1:p.Glu37Val
NR_103872.1:n.181_182delinsTG
NR_103872.2:n.152_153delinsTG
NR_103873.1:n.113+68_113+69delinsTG
ENST00000337432.8:c.110_111delinsTG ENSP00000336701.4:p.Glu37Val
ENST00000421782.3:c.110_111delinsTG ENSP00000391450.2:p.Glu37Val
ENST00000461271.5:c.-207+68_-207+69delinsTG ENSP00000464056.1:n.-207+68_-207+69delinsTG
ENST00000461271.6:c.-207+68_-207+69delinsTG ENSP00000464056.2:n.-207+68_-207+69delinsTG
ENST00000475762.5:c.110_111delinsTG ENSP00000432421.1:p.Glu37Val
ENST00000476741.2:n.152_153delinsTG
ENST00000482007.5:c.110_111delinsTG ENSP00000433332.1:p.Glu37Val
ENST00000486827.1:c.110_111delinsTG ENSP00000436761.1:p.Glu37Val
ENST00000487525.5:c.110_111delinsTG ENSP00000431637.1:p.Glu37Val
ENST00000487921.5:n.57+121_57+122delinsTG
ENST00000583539.5:c.110_111delinsTG ENSP00000463121.1:p.Glu37Val
ENST00000584617.5:c.91_92delinsTG
ENST00000697675.1:n.181_182delinsTG
ENST00000697676.1:n.170_171delinsTG
ENST00000697677.1:n.168_169delinsTG
ENST00000697678.1:n.47+121_47+122delinsTG
ENST00000697679.1:n.161_162delinsTG
ENST00000697680.1:c.110_111delinsTG ENSP00000513392.1:p.Glu37Val
ENST00000697681.1:c.110_111delinsTG ENSP00000513393.1:p.Glu37Val
ENST00000697683.1:c.110_111delinsTG ENSP00000513395.1:p.Glu37Val
ENST00000697684.1:n.170_171delinsTG
ENST00000697685.1:c.110_111delinsTG ENSP00000513396.1:p.Glu37Val
ENST00000697686.1:c.-207+121_-207+122delinsTG ENSP00000513397.1:n.-207+121_-207+122delinsTG
ENST00000697687.1:n.156_157delinsTG
ENST00000697688.1:n.156_157delinsTG
ENST00000697689.1:c.110_111delinsTG ENSP00000513398.1:p.Glu37Val
ENST00000697690.1:c.110_111delinsTG ENSP00000513399.1:p.Glu37Val
ENST00000697691.1:c.42+68_42+69delinsTG ENSP00000513400.1:n.42+68_42+69delinsTG
ENST00000697692.1:c.110_111delinsTG ENSP00000513401.1:p.Glu37Val
ENST00000697693.1:n.23_24delinsTG
XM_006722001.2:c.110_111delinsTG XP_006722064.1:p.Glu37Val
XM_006722001.4:c.110_111delinsTG XP_006722064.1:p.Glu37Val
XM_006722002.2:c.110_111delinsTG XP_006722065.1:p.Glu37Val
XM_006722002.4:c.110_111delinsTG XP_006722065.1:p.Glu37Val
XM_006722004.2:c.-207+68_-207+69delinsTG XP_006722067.1:n.-207+68_-207+69delinsTG
XM_006722004.3:c.-207+68_-207+69delinsTG XP_006722067.1:n.-207+68_-207+69delinsTG
XM_006722005.2:c.-207+121_-207+122delinsTG XP_006722068.1:n.-207+121_-207+122delinsTG
XM_006722005.3:c.-207+121_-207+122delinsTG XP_006722068.1:n.-207+121_-207+122delinsTG
XM_011525092.1:c.-507+68_-507+69delinsTG XP_011523394.1:n.-507+68_-507+69delinsTG
XM_011525092.2:c.-507+68_-507+69delinsTG XP_011523394.1:n.-507+68_-507+69delinsTG
XM_011525093.1:c.-668+68_-668+69delinsTG XP_011523395.1:n.-668+68_-668+69delinsTG
XM_011525093.2:c.-668+68_-668+69delinsTG XP_011523395.1:n.-668+68_-668+69delinsTG
XM_017024914.1:c.-207+68_-207+69delinsTG XP_016880403.1:n.-207+68_-207+69delinsTG
XM_017024916.1:c.-507+68_-507+69delinsTG XP_016880405.1:n.-507+68_-507+69delinsTG
XM_017024917.1:c.-207+121_-207+122delinsTG XP_016880406.1:n.-207+121_-207+122delinsTG
XM_017024918.2:c.-413_-412delinsTG XP_016880407.1:n.-413_-412delinsTG
XM_017024919.1:c.-668+68_-668+69delinsTG XP_016880408.1:n.-668+68_-668+69delinsTG
XR_934513.1:n.183_184delinsTG
XR_934513.3:n.614_615delinsTG
XR_934514.1:n.183_184delinsTG
XR_934514.3:n.614_615delinsTG