Canonical Allele Identifier: CA2267819516

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703325_58703327delinsCAA , CM000679.2:g.58703325_58703327delinsCAA	GRCh38
NC_000017.10:g.56780686_56780688delinsCAA , CM000679.1:g.56780686_56780688delinsCAA	GRCh37
NC_000017.9:g.54135685_54135687delinsCAA	NCBI36
NG_023199.1:g.15724_15726delinsCAA , LRG_314:g.15724_15726delinsCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.350_352delinsCAA	ENSP00000464056.2:p.Ser117=
ENST00000697677.1:n.1782_1784delinsCAA
ENST00000697678.1:n.603_605delinsCAA
ENST00000697679.1:n.1775_1777delinsCAA
ENST00000697680.1:c.*1565_*1567delinsCAA	ENSP00000513392.1:n.*1565_*1567delinsCAA
ENST00000697681.1:c.*1717_*1719delinsCAA	ENSP00000513393.1:n.*1717_*1719delinsCAA
ENST00000697683.1:c.*1565_*1567delinsCAA	ENSP00000513395.1:n.*1565_*1567delinsCAA
ENST00000697684.1:n.761_763delinsCAA
ENST00000697685.1:c.*1398_*1400delinsCAA	ENSP00000513396.1:n.*1398_*1400delinsCAA
ENST00000697686.1:c.350_352delinsCAA	ENSP00000513397.1:p.Ser117=
ENST00000697687.1:n.580_582delinsCAA
ENST00000697688.1:n.747_749delinsCAA
ENST00000697689.1:c.*1237_*1239delinsCAA	ENSP00000513398.1:n.*1237_*1239delinsCAA
ENST00000697690.1:c.701_703delinsCAA	ENSP00000513399.1:p.Ser234=
ENST00000697691.1:c.*673_*675delinsCAA	ENSP00000513400.1:n.*673_*675delinsCAA
ENST00000697692.1:c.*713_*715delinsCAA	ENSP00000513401.1:n.*713_*715delinsCAA
ENST00000697694.1:c.350_352delinsCAA	ENSP00000513402.1:p.Ser117=
ENST00000697695.1:n.1308_1310delinsCAA
ENST00000337432.9:c.701_703delinsCAA MANE Select	ENSP00000336701.4:p.Ser234=
ENST00000337432.8:c.701_703delinsCAA	ENSP00000336701.4:p.Ser234=
ENST00000413590.5:c.339_341delinsCAA
ENST00000425173.5:c.497_499delinsCAA	ENSP00000407282.1:p.Ser166=
ENST00000461271.5:c.350_352delinsCAA	ENSP00000464056.1:p.Ser117=
ENST00000475762.5:c.*1404_*1406delinsCAA	ENSP00000432421.1:n.*1404_*1406delinsCAA
ENST00000482007.5:c.*129_*131delinsCAA	ENSP00000433332.1:n.*129_*131delinsCAA
ENST00000487525.5:c.*129_*131delinsCAA	ENSP00000431637.1:n.*129_*131delinsCAA
ENST00000487921.5:n.613_615delinsCAA
ENST00000583539.5:c.701_703delinsCAA	ENSP00000463121.1:p.Ser234=
ENST00000584617.5:c.423_425delinsCAA
NM_058216.2:c.701_703delinsCAA	NP_478123.1:p.Ser234=
NR_103872.1:n.605_607delinsCAA
XM_006722001.2:c.701_703delinsCAA	XP_006722064.1:p.Ser234=
XM_006722002.2:c.701_703delinsCAA	XP_006722065.1:p.Ser234=
XM_006722004.2:c.350_352delinsCAA	XP_006722067.1:p.Ser117=
XM_006722005.2:c.350_352delinsCAA	XP_006722068.1:p.Ser117=
XM_011525092.1:c.350_352delinsCAA	XP_011523394.1:p.Ser117=
XM_011525093.1:c.350_352delinsCAA	XP_011523395.1:p.Ser117=
XM_011525094.1:c.350_352delinsCAA	XP_011523396.1:p.Ser117=
XR_934513.1:n.774_776delinsCAA
XR_934514.1:n.774_776delinsCAA
XM_006722001.4:c.701_703delinsCAA	XP_006722064.1:p.Ser234=
XM_006722002.4:c.701_703delinsCAA	XP_006722065.1:p.Ser234=
XM_006722004.3:c.350_352delinsCAA	XP_006722067.1:p.Ser117=
XM_006722005.3:c.350_352delinsCAA	XP_006722068.1:p.Ser117=
XM_011525092.2:c.350_352delinsCAA	XP_011523394.1:p.Ser117=
XM_011525093.2:c.350_352delinsCAA	XP_011523395.1:p.Ser117=
XM_011525094.2:c.350_352delinsCAA	XP_011523396.1:p.Ser117=
XM_017024914.1:c.350_352delinsCAA	XP_016880403.1:p.Ser117=
XM_017024915.1:c.350_352delinsCAA	XP_016880404.1:p.Ser117=
XM_017024916.1:c.350_352delinsCAA	XP_016880405.1:p.Ser117=
XM_017024917.1:c.350_352delinsCAA	XP_016880406.1:p.Ser117=
XM_017024918.2:c.350_352delinsCAA	XP_016880407.1:p.Ser117=
XM_017024919.1:c.350_352delinsCAA	XP_016880408.1:p.Ser117=
XR_934513.3:n.1205_1207delinsCAA
XR_934514.3:n.1205_1207delinsCAA
NM_058216.3:c.701_703delinsCAA MANE Select	NP_478123.1:p.Ser234=
NR_103872.2:n.576_578delinsCAA