Canonical Allele Identifier: CA3057228890
Community Standard Title: NM_058216.3(RAD51C):c.150_152delinsCGC (p.Gly51Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58694935_58694937delinsCGC , CM000679.2:g.58694935_58694937delinsCGC GRCh38
NC_000017.10:g.56772296_56772298delinsCGC , CM000679.1:g.56772296_56772298delinsCGC GRCh37
NC_000017.9:g.54127295_54127297delinsCGC NCBI36
NG_023199.1:g.7334_7336delinsCGC , LRG_314:g.7334_7336delinsCGC
NG_047169.1:g.2143_2145delinsGCG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.150_152delinsCGC MANE Select NP_478123.1:p.Gly51Ala
ENST00000337432.9:c.150_152delinsCGC MANE Select ENSP00000336701.4:p.Gly51Ala
NM_002876.3:c.150_152delinsCGC NP_002867.1:p.Gly51Ala
NM_002876.4:c.150_152delinsCGC NP_002867.1:p.Gly51Ala
NM_058216.2:c.150_152delinsCGC NP_478123.1:p.Gly51Ala
NR_103872.1:n.221_223delinsCGC
NR_103872.2:n.192_194delinsCGC
NR_103873.1:n.118_120delinsCGC
ENST00000337432.8:c.150_152delinsCGC ENSP00000336701.4:p.Gly51Ala
ENST00000421782.3:c.150_152delinsCGC ENSP00000391450.2:p.Gly51Ala
ENST00000461271.5:c.-202_-200delinsCGC ENSP00000464056.1:n.-202_-200delinsCGC
ENST00000461271.6:c.-202_-200delinsCGC ENSP00000464056.2:n.-202_-200delinsCGC
ENST00000475762.5:c.*853_*855delinsCGC ENSP00000432421.1:n.*853_*855delinsCGC
ENST00000482007.5:c.150_152delinsCGC ENSP00000433332.1:p.Gly51Ala
ENST00000486827.1:c.*1014_*1016delinsCGC ENSP00000436761.1:n.*1014_*1016delinsCGC
ENST00000487525.5:c.150_152delinsCGC ENSP00000431637.1:p.Gly51Ala
ENST00000487921.5:n.62_64delinsCGC
ENST00000583539.5:c.150_152delinsCGC ENSP00000463121.1:p.Gly51Ala
ENST00000584617.5:c.127-1758_127-1756delinsCGC
ENST00000697675.1:n.1244_1246delinsCGC
ENST00000697676.1:n.210_212delinsCGC
ENST00000697677.1:n.1231_1233delinsCGC
ENST00000697678.1:n.52_54delinsCGC
ENST00000697679.1:n.1224_1226delinsCGC
ENST00000697680.1:c.*1014_*1016delinsCGC ENSP00000513392.1:n.*1014_*1016delinsCGC
ENST00000697681.1:c.*1014_*1016delinsCGC ENSP00000513393.1:n.*1014_*1016delinsCGC
ENST00000697683.1:c.*1014_*1016delinsCGC ENSP00000513395.1:n.*1014_*1016delinsCGC
ENST00000697684.1:n.210_212delinsCGC
ENST00000697685.1:c.*1014_*1016delinsCGC ENSP00000513396.1:n.*1014_*1016delinsCGC
ENST00000697686.1:c.-202_-200delinsCGC ENSP00000513397.1:n.-202_-200delinsCGC
ENST00000697687.1:n.196_198delinsCGC
ENST00000697688.1:n.196_198delinsCGC
ENST00000697689.1:c.*853_*855delinsCGC ENSP00000513398.1:n.*853_*855delinsCGC
ENST00000697690.1:c.150_152delinsCGC ENSP00000513399.1:p.Gly51Ala
ENST00000697691.1:c.*122_*124delinsCGC ENSP00000513400.1:n.*122_*124delinsCGC
ENST00000697692.1:c.*162_*164delinsCGC ENSP00000513401.1:n.*162_*164delinsCGC
ENST00000697693.1:n.925_927delinsCGC
ENST00000697694.1:c.-202_-200delinsCGC ENSP00000513402.1:n.-202_-200delinsCGC
ENST00000697695.1:n.757_759delinsCGC
XM_006722001.2:c.150_152delinsCGC XP_006722064.1:p.Gly51Ala
XM_006722001.4:c.150_152delinsCGC XP_006722064.1:p.Gly51Ala
XM_006722002.2:c.150_152delinsCGC XP_006722065.1:p.Gly51Ala
XM_006722002.4:c.150_152delinsCGC XP_006722065.1:p.Gly51Ala
XM_006722004.2:c.-202_-200delinsCGC XP_006722067.1:n.-202_-200delinsCGC
XM_006722004.3:c.-202_-200delinsCGC XP_006722067.1:n.-202_-200delinsCGC
XM_006722005.2:c.-202_-200delinsCGC XP_006722068.1:n.-202_-200delinsCGC
XM_006722005.3:c.-202_-200delinsCGC XP_006722068.1:n.-202_-200delinsCGC
XM_011525092.1:c.-202_-200delinsCGC XP_011523394.1:n.-202_-200delinsCGC
XM_011525092.2:c.-202_-200delinsCGC XP_011523394.1:n.-202_-200delinsCGC
XM_011525093.1:c.-202_-200delinsCGC XP_011523395.1:n.-202_-200delinsCGC
XM_011525093.2:c.-202_-200delinsCGC XP_011523395.1:n.-202_-200delinsCGC
XM_011525094.1:c.-202_-200delinsCGC XP_011523396.1:n.-202_-200delinsCGC
XM_011525094.2:c.-202_-200delinsCGC XP_011523396.1:n.-202_-200delinsCGC
XM_017024914.1:c.-202_-200delinsCGC XP_016880403.1:n.-202_-200delinsCGC
XM_017024915.1:c.-202_-200delinsCGC XP_016880404.1:n.-202_-200delinsCGC
XM_017024916.1:c.-202_-200delinsCGC XP_016880405.1:n.-202_-200delinsCGC
XM_017024917.1:c.-202_-200delinsCGC XP_016880406.1:n.-202_-200delinsCGC
XM_017024918.2:c.-202_-200delinsCGC XP_016880407.1:n.-202_-200delinsCGC
XM_017024919.1:c.-202_-200delinsCGC XP_016880408.1:n.-202_-200delinsCGC
XR_934513.1:n.223_225delinsCGC
XR_934513.3:n.654_656delinsCGC
XR_934514.1:n.223_225delinsCGC
XR_934514.3:n.654_656delinsCGC