Canonical Allele Identifier: CA3261180241
Community Standard Title: NM_058216.3(RAD51C):c.685_687delinsCTG (p.Phe229Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703309_58703311delinsCTG , CM000679.2:g.58703309_58703311delinsCTG GRCh38
NC_000017.10:g.56780670_56780672delinsCTG , CM000679.1:g.56780670_56780672delinsCTG GRCh37
NC_000017.9:g.54135669_54135671delinsCTG NCBI36
NG_023199.1:g.15708_15710delinsCTG , LRG_314:g.15708_15710delinsCTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.685_687delinsCTG MANE Select NP_478123.1:p.Phe229Leu
ENST00000337432.9:c.685_687delinsCTG MANE Select ENSP00000336701.4:p.Phe229Leu
NM_058216.2:c.685_687delinsCTG NP_478123.1:p.Phe229Leu
NR_103872.1:n.589_591delinsCTG
NR_103872.2:n.560_562delinsCTG
ENST00000337432.8:c.685_687delinsCTG ENSP00000336701.4:p.Phe229Leu
ENST00000413590.5:c.323_325delinsCTG
ENST00000425173.5:c.481_483delinsCTG ENSP00000407282.1:p.Phe161Leu
ENST00000461271.5:c.334_336delinsCTG ENSP00000464056.1:p.Phe112Leu
ENST00000461271.6:c.334_336delinsCTG ENSP00000464056.2:p.Phe112Leu
ENST00000475762.5:c.*1388_*1390delinsCTG ENSP00000432421.1:n.*1388_*1390delinsCTG
ENST00000482007.5:c.*113_*115delinsCTG ENSP00000433332.1:n.*113_*115delinsCTG
ENST00000487525.5:c.*113_*115delinsCTG ENSP00000431637.1:n.*113_*115delinsCTG
ENST00000487921.5:n.597_599delinsCTG
ENST00000583539.5:c.685_687delinsCTG ENSP00000463121.1:p.Phe229Leu
ENST00000584617.5:c.407_409delinsCTG
ENST00000697677.1:n.1766_1768delinsCTG
ENST00000697678.1:n.587_589delinsCTG
ENST00000697679.1:n.1759_1761delinsCTG
ENST00000697680.1:c.*1549_*1551delinsCTG ENSP00000513392.1:n.*1549_*1551delinsCTG
ENST00000697681.1:c.*1701_*1703delinsCTG ENSP00000513393.1:n.*1701_*1703delinsCTG
ENST00000697683.1:c.*1549_*1551delinsCTG ENSP00000513395.1:n.*1549_*1551delinsCTG
ENST00000697684.1:n.745_747delinsCTG
ENST00000697685.1:c.*1382_*1384delinsCTG ENSP00000513396.1:n.*1382_*1384delinsCTG
ENST00000697686.1:c.334_336delinsCTG ENSP00000513397.1:p.Phe112Leu
ENST00000697687.1:n.564_566delinsCTG
ENST00000697688.1:n.731_733delinsCTG
ENST00000697689.1:c.*1221_*1223delinsCTG ENSP00000513398.1:n.*1221_*1223delinsCTG
ENST00000697690.1:c.685_687delinsCTG ENSP00000513399.1:p.Phe229Leu
ENST00000697691.1:c.*657_*659delinsCTG ENSP00000513400.1:n.*657_*659delinsCTG
ENST00000697692.1:c.*697_*699delinsCTG ENSP00000513401.1:n.*697_*699delinsCTG
ENST00000697694.1:c.334_336delinsCTG ENSP00000513402.1:p.Phe112Leu
ENST00000697695.1:n.1292_1294delinsCTG
XM_006722001.2:c.685_687delinsCTG XP_006722064.1:p.Phe229Leu
XM_006722001.4:c.685_687delinsCTG XP_006722064.1:p.Phe229Leu
XM_006722002.2:c.685_687delinsCTG XP_006722065.1:p.Phe229Leu
XM_006722002.4:c.685_687delinsCTG XP_006722065.1:p.Phe229Leu
XM_006722004.2:c.334_336delinsCTG XP_006722067.1:p.Phe112Leu
XM_006722004.3:c.334_336delinsCTG XP_006722067.1:p.Phe112Leu
XM_006722005.2:c.334_336delinsCTG XP_006722068.1:p.Phe112Leu
XM_006722005.3:c.334_336delinsCTG XP_006722068.1:p.Phe112Leu
XM_011525092.1:c.334_336delinsCTG XP_011523394.1:p.Phe112Leu
XM_011525092.2:c.334_336delinsCTG XP_011523394.1:p.Phe112Leu
XM_011525093.1:c.334_336delinsCTG XP_011523395.1:p.Phe112Leu
XM_011525093.2:c.334_336delinsCTG XP_011523395.1:p.Phe112Leu
XM_011525094.1:c.334_336delinsCTG XP_011523396.1:p.Phe112Leu
XM_011525094.2:c.334_336delinsCTG XP_011523396.1:p.Phe112Leu
XM_017024914.1:c.334_336delinsCTG XP_016880403.1:p.Phe112Leu
XM_017024915.1:c.334_336delinsCTG XP_016880404.1:p.Phe112Leu
XM_017024916.1:c.334_336delinsCTG XP_016880405.1:p.Phe112Leu
XM_017024917.1:c.334_336delinsCTG XP_016880406.1:p.Phe112Leu
XM_017024918.2:c.334_336delinsCTG XP_016880407.1:p.Phe112Leu
XM_017024919.1:c.334_336delinsCTG XP_016880408.1:p.Phe112Leu
XR_934513.1:n.758_760delinsCTG
XR_934513.3:n.1189_1191delinsCTG
XR_934514.1:n.758_760delinsCTG
XR_934514.3:n.1189_1191delinsCTG