Canonical Allele Identifier: CA3261180696
Community Standard Title: NM_058216.3(RAD51C):c.154_156delinsCTG (p.Ile52Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58694939_58694941delinsCTG , CM000679.2:g.58694939_58694941delinsCTG GRCh38
NC_000017.10:g.56772300_56772302delinsCTG , CM000679.1:g.56772300_56772302delinsCTG GRCh37
NC_000017.9:g.54127299_54127301delinsCTG NCBI36
NG_023199.1:g.7338_7340delinsCTG , LRG_314:g.7338_7340delinsCTG
NG_047169.1:g.2139_2141delinsCAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.154_156delinsCTG MANE Select NP_478123.1:p.Ile52Leu
ENST00000337432.9:c.154_156delinsCTG MANE Select ENSP00000336701.4:p.Ile52Leu
NM_002876.3:c.154_156delinsCTG NP_002867.1:p.Ile52Leu
NM_002876.4:c.154_156delinsCTG NP_002867.1:p.Ile52Leu
NM_058216.2:c.154_156delinsCTG NP_478123.1:p.Ile52Leu
NR_103872.1:n.225_227delinsCTG
NR_103872.2:n.196_198delinsCTG
NR_103873.1:n.122_124delinsCTG
ENST00000337432.8:c.154_156delinsCTG ENSP00000336701.4:p.Ile52Leu
ENST00000421782.3:c.154_156delinsCTG ENSP00000391450.2:p.Ile52Leu
ENST00000461271.5:c.-198_-196delinsCTG ENSP00000464056.1:n.-198_-196delinsCTG
ENST00000461271.6:c.-198_-196delinsCTG ENSP00000464056.2:n.-198_-196delinsCTG
ENST00000475762.5:c.*857_*859delinsCTG ENSP00000432421.1:n.*857_*859delinsCTG
ENST00000482007.5:c.154_156delinsCTG ENSP00000433332.1:p.Ile52Leu
ENST00000486827.1:c.*1018_*1020delinsCTG ENSP00000436761.1:n.*1018_*1020delinsCTG
ENST00000487525.5:c.154_156delinsCTG ENSP00000431637.1:p.Ile52Leu
ENST00000487921.5:n.66_68delinsCTG
ENST00000583539.5:c.154_156delinsCTG ENSP00000463121.1:p.Ile52Leu
ENST00000584617.5:c.127-1754_127-1752delinsCTG
ENST00000697675.1:n.1248_1250delinsCTG
ENST00000697676.1:n.214_216delinsCTG
ENST00000697677.1:n.1235_1237delinsCTG
ENST00000697678.1:n.56_58delinsCTG
ENST00000697679.1:n.1228_1230delinsCTG
ENST00000697680.1:c.*1018_*1020delinsCTG ENSP00000513392.1:n.*1018_*1020delinsCTG
ENST00000697681.1:c.*1018_*1020delinsCTG ENSP00000513393.1:n.*1018_*1020delinsCTG
ENST00000697683.1:c.*1018_*1020delinsCTG ENSP00000513395.1:n.*1018_*1020delinsCTG
ENST00000697684.1:n.214_216delinsCTG
ENST00000697685.1:c.*1018_*1020delinsCTG ENSP00000513396.1:n.*1018_*1020delinsCTG
ENST00000697686.1:c.-198_-196delinsCTG ENSP00000513397.1:n.-198_-196delinsCTG
ENST00000697687.1:n.200_202delinsCTG
ENST00000697688.1:n.200_202delinsCTG
ENST00000697689.1:c.*857_*859delinsCTG ENSP00000513398.1:n.*857_*859delinsCTG
ENST00000697690.1:c.154_156delinsCTG ENSP00000513399.1:p.Ile52Leu
ENST00000697691.1:c.*126_*128delinsCTG ENSP00000513400.1:n.*126_*128delinsCTG
ENST00000697692.1:c.*166_*168delinsCTG ENSP00000513401.1:n.*166_*168delinsCTG
ENST00000697693.1:n.929_931delinsCTG
ENST00000697694.1:c.-198_-196delinsCTG ENSP00000513402.1:n.-198_-196delinsCTG
ENST00000697695.1:n.761_763delinsCTG
XM_006722001.2:c.154_156delinsCTG XP_006722064.1:p.Ile52Leu
XM_006722001.4:c.154_156delinsCTG XP_006722064.1:p.Ile52Leu
XM_006722002.2:c.154_156delinsCTG XP_006722065.1:p.Ile52Leu
XM_006722002.4:c.154_156delinsCTG XP_006722065.1:p.Ile52Leu
XM_006722004.2:c.-198_-196delinsCTG XP_006722067.1:n.-198_-196delinsCTG
XM_006722004.3:c.-198_-196delinsCTG XP_006722067.1:n.-198_-196delinsCTG
XM_006722005.2:c.-198_-196delinsCTG XP_006722068.1:n.-198_-196delinsCTG
XM_006722005.3:c.-198_-196delinsCTG XP_006722068.1:n.-198_-196delinsCTG
XM_011525092.1:c.-198_-196delinsCTG XP_011523394.1:n.-198_-196delinsCTG
XM_011525092.2:c.-198_-196delinsCTG XP_011523394.1:n.-198_-196delinsCTG
XM_011525093.1:c.-198_-196delinsCTG XP_011523395.1:n.-198_-196delinsCTG
XM_011525093.2:c.-198_-196delinsCTG XP_011523395.1:n.-198_-196delinsCTG
XM_011525094.1:c.-198_-196delinsCTG XP_011523396.1:n.-198_-196delinsCTG
XM_011525094.2:c.-198_-196delinsCTG XP_011523396.1:n.-198_-196delinsCTG
XM_017024914.1:c.-198_-196delinsCTG XP_016880403.1:n.-198_-196delinsCTG
XM_017024915.1:c.-198_-196delinsCTG XP_016880404.1:n.-198_-196delinsCTG
XM_017024916.1:c.-198_-196delinsCTG XP_016880405.1:n.-198_-196delinsCTG
XM_017024917.1:c.-198_-196delinsCTG XP_016880406.1:n.-198_-196delinsCTG
XM_017024918.2:c.-198_-196delinsCTG XP_016880407.1:n.-198_-196delinsCTG
XM_017024919.1:c.-198_-196delinsCTG XP_016880408.1:n.-198_-196delinsCTG
XR_934513.1:n.227_229delinsCTG
XR_934513.3:n.658_660delinsCTG
XR_934514.1:n.227_229delinsCTG
XR_934514.3:n.658_660delinsCTG