Canonical Allele Identifier: CA3261179912
Community Standard Title: NM_058216.3(RAD51C):c.787_789delinsCAC (p.Asn263His)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709940_58709942delinsCAC , CM000679.2:g.58709940_58709942delinsCAC GRCh38
NC_000017.10:g.56787301_56787303delinsCAC , CM000679.1:g.56787301_56787303delinsCAC GRCh37
NC_000017.9:g.54142300_54142302delinsCAC NCBI36
NG_023199.1:g.22339_22341delinsCAC , LRG_314:g.22339_22341delinsCAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.787_789delinsCAC MANE Select NP_478123.1:p.Asn263His
ENST00000337432.9:c.787_789delinsCAC MANE Select ENSP00000336701.4:p.Asn263His
NM_058216.2:c.787_789delinsCAC NP_478123.1:p.Asn263His
NR_103872.1:n.691_693delinsCAC
NR_103872.2:n.662_664delinsCAC
ENST00000337432.8:c.787_789delinsCAC ENSP00000336701.4:p.Asn263His
ENST00000413590.5:c.425_427delinsCAC
ENST00000461271.6:c.436_438delinsCAC ENSP00000464056.2:p.Asn146His
ENST00000475762.5:c.*1490_*1492delinsCAC ENSP00000432421.1:n.*1490_*1492delinsCAC
ENST00000482007.5:c.*215_*217delinsCAC ENSP00000433332.1:n.*215_*217delinsCAC
ENST00000487525.5:c.*360_*362delinsCAC ENSP00000431637.1:n.*360_*362delinsCAC
ENST00000578151.1:n.122_124delinsCAC
ENST00000581221.5:n.302_304delinsCAC
ENST00000583539.5:c.787_789delinsCAC ENSP00000463121.1:p.Asn263His
ENST00000584617.5:c.509_511delinsCAC
ENST00000584804.1:c.82_84delinsCAC ENSP00000463658.1:p.Asn28His
ENST00000697678.1:n.689_691delinsCAC
ENST00000697679.1:n.1861_1863delinsCAC
ENST00000697680.1:c.*1651_*1653delinsCAC ENSP00000513392.1:n.*1651_*1653delinsCAC
ENST00000697681.1:c.*1948_*1950delinsCAC ENSP00000513393.1:n.*1948_*1950delinsCAC
ENST00000697683.1:c.*1651_*1653delinsCAC ENSP00000513395.1:n.*1651_*1653delinsCAC
ENST00000697684.1:n.847_849delinsCAC
ENST00000697685.1:c.*1484_*1486delinsCAC ENSP00000513396.1:n.*1484_*1486delinsCAC
ENST00000697686.1:c.436_438delinsCAC ENSP00000513397.1:p.Asn146His
ENST00000697687.1:n.666_668delinsCAC
ENST00000697688.1:n.833_835delinsCAC
ENST00000697689.1:c.*1323_*1325delinsCAC ENSP00000513398.1:n.*1323_*1325delinsCAC
ENST00000697690.1:c.787_789delinsCAC ENSP00000513399.1:p.Asn263His
ENST00000697691.1:c.*759_*761delinsCAC ENSP00000513400.1:n.*759_*761delinsCAC
ENST00000697692.1:c.*799_*801delinsCAC ENSP00000513401.1:n.*799_*801delinsCAC
ENST00000697694.1:c.436_438delinsCAC ENSP00000513402.1:p.Asn146His
ENST00000697695.1:n.1394_1396delinsCAC
XM_006722001.2:c.787_789delinsCAC XP_006722064.1:p.Asn263His
XM_006722001.4:c.787_789delinsCAC XP_006722064.1:p.Asn263His
XM_006722002.2:c.787_789delinsCAC XP_006722065.1:p.Asn263His
XM_006722002.4:c.787_789delinsCAC XP_006722065.1:p.Asn263His
XM_006722004.2:c.436_438delinsCAC XP_006722067.1:p.Asn146His
XM_006722004.3:c.436_438delinsCAC XP_006722067.1:p.Asn146His
XM_006722005.2:c.436_438delinsCAC XP_006722068.1:p.Asn146His
XM_006722005.3:c.436_438delinsCAC XP_006722068.1:p.Asn146His
XM_011525092.1:c.436_438delinsCAC XP_011523394.1:p.Asn146His
XM_011525092.2:c.436_438delinsCAC XP_011523394.1:p.Asn146His
XM_011525093.1:c.436_438delinsCAC XP_011523395.1:p.Asn146His
XM_011525093.2:c.436_438delinsCAC XP_011523395.1:p.Asn146His
XM_011525094.1:c.436_438delinsCAC XP_011523396.1:p.Asn146His
XM_011525094.2:c.436_438delinsCAC XP_011523396.1:p.Asn146His
XM_017024914.1:c.436_438delinsCAC XP_016880403.1:p.Asn146His
XM_017024915.1:c.436_438delinsCAC XP_016880404.1:p.Asn146His
XM_017024916.1:c.436_438delinsCAC XP_016880405.1:p.Asn146His
XM_017024917.1:c.436_438delinsCAC XP_016880406.1:p.Asn146His
XM_017024918.2:c.436_438delinsCAC XP_016880407.1:p.Asn146His
XM_017024919.1:c.436_438delinsCAC XP_016880408.1:p.Asn146His
XR_934513.1:n.1005_1007delinsCAC
XR_934513.3:n.1436_1438delinsCAC
XR_934514.1:n.1005_1007delinsCAC
XR_934514.3:n.1436_1438delinsCAC