Canonical Allele Identifier: CA3261180275
Community Standard Title: NM_058216.3(RAD51C):c.685_687delinsCTT (p.Phe229Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703309_58703311delinsCTT , CM000679.2:g.58703309_58703311delinsCTT GRCh38
NC_000017.10:g.56780670_56780672delinsCTT , CM000679.1:g.56780670_56780672delinsCTT GRCh37
NC_000017.9:g.54135669_54135671delinsCTT NCBI36
NG_023199.1:g.15708_15710delinsCTT , LRG_314:g.15708_15710delinsCTT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.685_687delinsCTT MANE Select NP_478123.1:p.Phe229Leu
ENST00000337432.9:c.685_687delinsCTT MANE Select ENSP00000336701.4:p.Phe229Leu
NM_058216.2:c.685_687delinsCTT NP_478123.1:p.Phe229Leu
NR_103872.1:n.589_591delinsCTT
NR_103872.2:n.560_562delinsCTT
ENST00000337432.8:c.685_687delinsCTT ENSP00000336701.4:p.Phe229Leu
ENST00000413590.5:c.323_325delinsCTT
ENST00000425173.5:c.481_483delinsCTT ENSP00000407282.1:p.Phe161Leu
ENST00000461271.5:c.334_336delinsCTT ENSP00000464056.1:p.Phe112Leu
ENST00000461271.6:c.334_336delinsCTT ENSP00000464056.2:p.Phe112Leu
ENST00000475762.5:c.*1388_*1390delinsCTT ENSP00000432421.1:n.*1388_*1390delinsCTT
ENST00000482007.5:c.*113_*115delinsCTT ENSP00000433332.1:n.*113_*115delinsCTT
ENST00000487525.5:c.*113_*115delinsCTT ENSP00000431637.1:n.*113_*115delinsCTT
ENST00000487921.5:n.597_599delinsCTT
ENST00000583539.5:c.685_687delinsCTT ENSP00000463121.1:p.Phe229Leu
ENST00000584617.5:c.407_409delinsCTT
ENST00000697677.1:n.1766_1768delinsCTT
ENST00000697678.1:n.587_589delinsCTT
ENST00000697679.1:n.1759_1761delinsCTT
ENST00000697680.1:c.*1549_*1551delinsCTT ENSP00000513392.1:n.*1549_*1551delinsCTT
ENST00000697681.1:c.*1701_*1703delinsCTT ENSP00000513393.1:n.*1701_*1703delinsCTT
ENST00000697683.1:c.*1549_*1551delinsCTT ENSP00000513395.1:n.*1549_*1551delinsCTT
ENST00000697684.1:n.745_747delinsCTT
ENST00000697685.1:c.*1382_*1384delinsCTT ENSP00000513396.1:n.*1382_*1384delinsCTT
ENST00000697686.1:c.334_336delinsCTT ENSP00000513397.1:p.Phe112Leu
ENST00000697687.1:n.564_566delinsCTT
ENST00000697688.1:n.731_733delinsCTT
ENST00000697689.1:c.*1221_*1223delinsCTT ENSP00000513398.1:n.*1221_*1223delinsCTT
ENST00000697690.1:c.685_687delinsCTT ENSP00000513399.1:p.Phe229Leu
ENST00000697691.1:c.*657_*659delinsCTT ENSP00000513400.1:n.*657_*659delinsCTT
ENST00000697692.1:c.*697_*699delinsCTT ENSP00000513401.1:n.*697_*699delinsCTT
ENST00000697694.1:c.334_336delinsCTT ENSP00000513402.1:p.Phe112Leu
ENST00000697695.1:n.1292_1294delinsCTT
XM_006722001.2:c.685_687delinsCTT XP_006722064.1:p.Phe229Leu
XM_006722001.4:c.685_687delinsCTT XP_006722064.1:p.Phe229Leu
XM_006722002.2:c.685_687delinsCTT XP_006722065.1:p.Phe229Leu
XM_006722002.4:c.685_687delinsCTT XP_006722065.1:p.Phe229Leu
XM_006722004.2:c.334_336delinsCTT XP_006722067.1:p.Phe112Leu
XM_006722004.3:c.334_336delinsCTT XP_006722067.1:p.Phe112Leu
XM_006722005.2:c.334_336delinsCTT XP_006722068.1:p.Phe112Leu
XM_006722005.3:c.334_336delinsCTT XP_006722068.1:p.Phe112Leu
XM_011525092.1:c.334_336delinsCTT XP_011523394.1:p.Phe112Leu
XM_011525092.2:c.334_336delinsCTT XP_011523394.1:p.Phe112Leu
XM_011525093.1:c.334_336delinsCTT XP_011523395.1:p.Phe112Leu
XM_011525093.2:c.334_336delinsCTT XP_011523395.1:p.Phe112Leu
XM_011525094.1:c.334_336delinsCTT XP_011523396.1:p.Phe112Leu
XM_011525094.2:c.334_336delinsCTT XP_011523396.1:p.Phe112Leu
XM_017024914.1:c.334_336delinsCTT XP_016880403.1:p.Phe112Leu
XM_017024915.1:c.334_336delinsCTT XP_016880404.1:p.Phe112Leu
XM_017024916.1:c.334_336delinsCTT XP_016880405.1:p.Phe112Leu
XM_017024917.1:c.334_336delinsCTT XP_016880406.1:p.Phe112Leu
XM_017024918.2:c.334_336delinsCTT XP_016880407.1:p.Phe112Leu
XM_017024919.1:c.334_336delinsCTT XP_016880408.1:p.Phe112Leu
XR_934513.1:n.758_760delinsCTT
XR_934513.3:n.1189_1191delinsCTT
XR_934514.1:n.758_760delinsCTT
XR_934514.3:n.1189_1191delinsCTT