Canonical Allele Identifier: CA2267815222

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694971_58694974delinsAATT , CM000679.2:g.58694971_58694974delinsAATT	GRCh38
NC_000017.10:g.56772332_56772335delinsAATT , CM000679.1:g.56772332_56772335delinsAATT	GRCh37
NC_000017.9:g.54127331_54127334delinsAATT	NCBI36
NG_023199.1:g.7370_7373delinsAATT , LRG_314:g.7370_7373delinsAATT
NG_047169.1:g.2106_2109delinsAATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-166_-163delinsAATT	ENSP00000464056.2:n.-166_-163delinsAATT
ENST00000697675.1:n.1280_1283delinsAATT
ENST00000697676.1:n.246_249delinsAATT
ENST00000697677.1:n.1267_1270delinsAATT
ENST00000697678.1:n.88_91delinsAATT
ENST00000697679.1:n.1260_1263delinsAATT
ENST00000697680.1:c.*1050_*1053delinsAATT	ENSP00000513392.1:n.*1050_*1053delinsAATT...
ENST00000697681.1:c.*1050_*1053delinsAATT	ENSP00000513393.1:n.*1050_*1053delinsAATT...
ENST00000697683.1:c.*1050_*1053delinsAATT	ENSP00000513395.1:n.*1050_*1053delinsAATT...
ENST00000697684.1:n.246_249delinsAATT
ENST00000697685.1:c.*1050_*1053delinsAATT	ENSP00000513396.1:n.*1050_*1053delinsAATT...
ENST00000697686.1:c.-166_-163delinsAATT	ENSP00000513397.1:n.-166_-163delinsAATT
ENST00000697687.1:n.232_235delinsAATT
ENST00000697688.1:n.232_235delinsAATT
ENST00000697689.1:c.*889_*892delinsAATT	ENSP00000513398.1:n.*889_*892delinsAATT
ENST00000697690.1:c.186_189delinsAATT	ENSP00000513399.1:p.Gln62=
ENST00000697691.1:c.*158_*161delinsAATT	ENSP00000513400.1:n.*158_*161delinsAATT
ENST00000697692.1:c.*198_*201delinsAATT	ENSP00000513401.1:n.*198_*201delinsAATT
ENST00000697693.1:n.961_964delinsAATT
ENST00000697694.1:c.-166_-163delinsAATT	ENSP00000513402.1:n.-166_-163delinsAATT
ENST00000697695.1:n.793_796delinsAATT
ENST00000337432.9:c.186_189delinsAATT MANE Select	ENSP00000336701.4:p.Gln62=
ENST00000337432.8:c.186_189delinsAATT	ENSP00000336701.4:p.Gln62=
ENST00000421782.3:c.186_189delinsAATT	ENSP00000391450.2:p.Gln62=
ENST00000461271.5:c.-166_-163delinsAATT	ENSP00000464056.1:n.-166_-163delinsAATT
ENST00000475762.5:c.*889_*892delinsAATT	ENSP00000432421.1:n.*889_*892delinsAATT
ENST00000482007.5:c.186_189delinsAATT	ENSP00000433332.1:p.Gln62=
ENST00000486827.1:c.*1050_*1053delinsAATT	ENSP00000436761.1:n.*1050_*1053delinsAATT...
ENST00000487525.5:c.186_189delinsAATT	ENSP00000431637.1:p.Gln62=
ENST00000487921.5:n.98_101delinsAATT
ENST00000583539.5:c.186_189delinsAATT	ENSP00000463121.1:p.Gln62=
ENST00000584617.5:c.127-1722_127-1719delinsAATT
NM_002876.3:c.186_189delinsAATT	NP_002867.1:p.Gln62=
NM_058216.2:c.186_189delinsAATT	NP_478123.1:p.Gln62=
NR_103872.1:n.257_260delinsAATT
NR_103873.1:n.154_157delinsAATT
XM_006722001.2:c.186_189delinsAATT	XP_006722064.1:p.Gln62=
XM_006722002.2:c.186_189delinsAATT	XP_006722065.1:p.Gln62=
XM_006722004.2:c.-166_-163delinsAATT	XP_006722067.1:n.-166_-163delinsAATT
XM_006722005.2:c.-166_-163delinsAATT	XP_006722068.1:n.-166_-163delinsAATT
XM_011525092.1:c.-166_-163delinsAATT	XP_011523394.1:n.-166_-163delinsAATT
XM_011525093.1:c.-166_-163delinsAATT	XP_011523395.1:n.-166_-163delinsAATT
XM_011525094.1:c.-166_-163delinsAATT	XP_011523396.1:n.-166_-163delinsAATT
XR_934513.1:n.259_262delinsAATT
XR_934514.1:n.259_262delinsAATT
XM_006722001.4:c.186_189delinsAATT	XP_006722064.1:p.Gln62=
XM_006722002.4:c.186_189delinsAATT	XP_006722065.1:p.Gln62=
XM_006722004.3:c.-166_-163delinsAATT	XP_006722067.1:n.-166_-163delinsAATT
XM_006722005.3:c.-166_-163delinsAATT	XP_006722068.1:n.-166_-163delinsAATT
XM_011525092.2:c.-166_-163delinsAATT	XP_011523394.1:n.-166_-163delinsAATT
XM_011525093.2:c.-166_-163delinsAATT	XP_011523395.1:n.-166_-163delinsAATT
XM_011525094.2:c.-166_-163delinsAATT	XP_011523396.1:n.-166_-163delinsAATT
XM_017024914.1:c.-166_-163delinsAATT	XP_016880403.1:n.-166_-163delinsAATT
XM_017024915.1:c.-166_-163delinsAATT	XP_016880404.1:n.-166_-163delinsAATT
XM_017024916.1:c.-166_-163delinsAATT	XP_016880405.1:n.-166_-163delinsAATT
XM_017024917.1:c.-166_-163delinsAATT	XP_016880406.1:n.-166_-163delinsAATT
XM_017024918.2:c.-166_-163delinsAATT	XP_016880407.1:n.-166_-163delinsAATT
XM_017024919.1:c.-166_-163delinsAATT	XP_016880408.1:n.-166_-163delinsAATT
XR_934513.3:n.690_693delinsAATT
XR_934514.3:n.690_693delinsAATT
NM_058216.3:c.186_189delinsAATT MANE Select	NP_478123.1:p.Gln62=
NR_103872.2:n.228_231delinsAATT
NM_002876.4:c.186_189delinsAATT	NP_002867.1:p.Gln62=