Canonical Allele Identifier: CA3261181212
Community Standard Title: NM_058216.3(RAD51C):c.241_243delinsCTG (p.Ser81Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695026_58695028delinsCTG , CM000679.2:g.58695026_58695028delinsCTG GRCh38
NC_000017.10:g.56772387_56772389delinsCTG , CM000679.1:g.56772387_56772389delinsCTG GRCh37
NC_000017.9:g.54127386_54127388delinsCTG NCBI36
NG_023199.1:g.7425_7427delinsCTG , LRG_314:g.7425_7427delinsCTG
NG_047169.1:g.2052_2054delinsCAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.241_243delinsCTG MANE Select NP_478123.1:p.Ser81Leu
ENST00000337432.9:c.241_243delinsCTG MANE Select ENSP00000336701.4:p.Ser81Leu
NM_002876.3:c.241_243delinsCTG NP_002867.1:p.Ser81Leu
NM_002876.4:c.241_243delinsCTG NP_002867.1:p.Ser81Leu
NM_058216.2:c.241_243delinsCTG NP_478123.1:p.Ser81Leu
NR_103872.1:n.312_314delinsCTG
NR_103872.2:n.283_285delinsCTG
NR_103873.1:n.209_211delinsCTG
ENST00000337432.8:c.241_243delinsCTG ENSP00000336701.4:p.Ser81Leu
ENST00000421782.3:c.241_243delinsCTG ENSP00000391450.2:p.Ser81Leu
ENST00000425173.5:c.37_39delinsCTG ENSP00000407282.1:p.Ser13Leu
ENST00000461271.5:c.-111_-109delinsCTG ENSP00000464056.1:n.-111_-109delinsCTG
ENST00000461271.6:c.-111_-109delinsCTG ENSP00000464056.2:n.-111_-109delinsCTG
ENST00000475762.5:c.*944_*946delinsCTG ENSP00000432421.1:n.*944_*946delinsCTG
ENST00000482007.5:c.241_243delinsCTG ENSP00000433332.1:p.Ser81Leu
ENST00000486827.1:c.*1105_*1107delinsCTG ENSP00000436761.1:n.*1105_*1107delinsCTG
ENST00000487525.5:c.241_243delinsCTG ENSP00000431637.1:p.Ser81Leu
ENST00000487921.5:n.153_155delinsCTG
ENST00000583539.5:c.241_243delinsCTG ENSP00000463121.1:p.Ser81Leu
ENST00000584617.5:c.127-1667_127-1665delinsCTG
ENST00000697675.1:n.1335_1337delinsCTG
ENST00000697676.1:n.301_303delinsCTG
ENST00000697677.1:n.1322_1324delinsCTG
ENST00000697678.1:n.143_145delinsCTG
ENST00000697679.1:n.1315_1317delinsCTG
ENST00000697680.1:c.*1105_*1107delinsCTG ENSP00000513392.1:n.*1105_*1107delinsCTG
ENST00000697681.1:c.*1105_*1107delinsCTG ENSP00000513393.1:n.*1105_*1107delinsCTG
ENST00000697683.1:c.*1105_*1107delinsCTG ENSP00000513395.1:n.*1105_*1107delinsCTG
ENST00000697684.1:n.301_303delinsCTG
ENST00000697685.1:c.*1105_*1107delinsCTG ENSP00000513396.1:n.*1105_*1107delinsCTG
ENST00000697686.1:c.-111_-109delinsCTG ENSP00000513397.1:n.-111_-109delinsCTG
ENST00000697687.1:n.287_289delinsCTG
ENST00000697688.1:n.287_289delinsCTG
ENST00000697689.1:c.*944_*946delinsCTG ENSP00000513398.1:n.*944_*946delinsCTG
ENST00000697690.1:c.241_243delinsCTG ENSP00000513399.1:p.Ser81Leu
ENST00000697691.1:c.*213_*215delinsCTG ENSP00000513400.1:n.*213_*215delinsCTG
ENST00000697692.1:c.*253_*255delinsCTG ENSP00000513401.1:n.*253_*255delinsCTG
ENST00000697693.1:n.1016_1018delinsCTG
ENST00000697694.1:c.-111_-109delinsCTG ENSP00000513402.1:n.-111_-109delinsCTG
ENST00000697695.1:n.848_850delinsCTG
XM_006722001.2:c.241_243delinsCTG XP_006722064.1:p.Ser81Leu
XM_006722001.4:c.241_243delinsCTG XP_006722064.1:p.Ser81Leu
XM_006722002.2:c.241_243delinsCTG XP_006722065.1:p.Ser81Leu
XM_006722002.4:c.241_243delinsCTG XP_006722065.1:p.Ser81Leu
XM_006722004.2:c.-111_-109delinsCTG XP_006722067.1:n.-111_-109delinsCTG
XM_006722004.3:c.-111_-109delinsCTG XP_006722067.1:n.-111_-109delinsCTG
XM_006722005.2:c.-111_-109delinsCTG XP_006722068.1:n.-111_-109delinsCTG
XM_006722005.3:c.-111_-109delinsCTG XP_006722068.1:n.-111_-109delinsCTG
XM_011525092.1:c.-111_-109delinsCTG XP_011523394.1:n.-111_-109delinsCTG
XM_011525092.2:c.-111_-109delinsCTG XP_011523394.1:n.-111_-109delinsCTG
XM_011525093.1:c.-111_-109delinsCTG XP_011523395.1:n.-111_-109delinsCTG
XM_011525093.2:c.-111_-109delinsCTG XP_011523395.1:n.-111_-109delinsCTG
XM_011525094.1:c.-111_-109delinsCTG XP_011523396.1:n.-111_-109delinsCTG
XM_011525094.2:c.-111_-109delinsCTG XP_011523396.1:n.-111_-109delinsCTG
XM_017024914.1:c.-111_-109delinsCTG XP_016880403.1:n.-111_-109delinsCTG
XM_017024915.1:c.-111_-109delinsCTG XP_016880404.1:n.-111_-109delinsCTG
XM_017024916.1:c.-111_-109delinsCTG XP_016880405.1:n.-111_-109delinsCTG
XM_017024917.1:c.-111_-109delinsCTG XP_016880406.1:n.-111_-109delinsCTG
XM_017024918.2:c.-111_-109delinsCTG XP_016880407.1:n.-111_-109delinsCTG
XM_017024919.1:c.-111_-109delinsCTG XP_016880408.1:n.-111_-109delinsCTG
XR_934513.1:n.314_316delinsCTG
XR_934513.3:n.745_747delinsCTG
XR_934514.1:n.314_316delinsCTG
XR_934514.3:n.745_747delinsCTG