Canonical Allele Identifier: CA985028388

Gene: RAD51C

Linked Data

• dbSNP Id: rs2048283250
• gnomAD v3: 17-58703573-A-ATAGC
• gnomAD v4: 17-58703573-A-ATAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703575_58703578dup , CM000679.2:g.58703575_58703578dup	GRCh38
NC_000017.10:g.56780936_56780939dup , CM000679.1:g.56780936_56780939dup	GRCh37
NC_000017.9:g.54135935_54135938dup	NCBI36
NG_023199.1:g.15974_15977dup , LRG_314:g.15974_15977dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.354+246_354+249dup	ENSP00000464056.2:n.354+246_354+249dup
ENST00000697677.1:n.2032_2035dup
ENST00000697678.1:n.607+246_607+249dup
ENST00000697679.1:n.1779+246_1779+249dup
ENST00000697680.1:c.*1569+246_*1569+249dup	ENSP00000513392.1:n.*1569+246_*1569+249dup
ENST00000697681.1:c.*1721+246_*1721+249dup	ENSP00000513393.1:n.*1721+246_*1721+249dup
ENST00000697683.1:c.*1569+246_*1569+249dup	ENSP00000513395.1:n.*1569+246_*1569+249dup
ENST00000697684.1:n.765+246_765+249dup
ENST00000697685.1:c.*1402+246_*1402+249dup	ENSP00000513396.1:n.*1402+246_*1402+249dup
ENST00000697686.1:c.354+246_354+249dup	ENSP00000513397.1:n.354+246_354+249dup
ENST00000697687.1:n.584+246_584+249dup
ENST00000697688.1:n.751+246_751+249dup
ENST00000697689.1:c.*1241+246_*1241+249dup	ENSP00000513398.1:n.*1241+246_*1241+249dup
ENST00000697690.1:c.705+246_705+249dup	ENSP00000513399.1:n.705+246_705+249dup
ENST00000697691.1:c.*677+246_*677+249dup	ENSP00000513400.1:n.*677+246_*677+249dup
ENST00000697692.1:c.*717+246_*717+249dup	ENSP00000513401.1:n.*717+246_*717+249dup
ENST00000697694.1:c.354+246_354+249dup	ENSP00000513402.1:n.354+246_354+249dup
ENST00000697695.1:n.1312+246_1312+249dup
ENST00000337432.9:c.705+246_705+249dup MANE Select	ENSP00000336701.4:n.705+246_705+249dup
ENST00000337432.8:c.705+246_705+249dup	ENSP00000336701.4:n.705+246_705+249dup
ENST00000413590.5:c.343+246_343+249dup
ENST00000425173.5:c.501+246_501+249dup	ENSP00000407282.1:n.501+246_501+249dup
ENST00000461271.5:c.354+246_354+249dup	ENSP00000464056.1:n.354+246_354+249dup
ENST00000475762.5:c.*1408+246_*1408+249dup	ENSP00000432421.1:n.*1408+246_*1408+249dup
ENST00000482007.5:c.*133+246_*133+249dup	ENSP00000433332.1:n.*133+246_*133+249dup
ENST00000487525.5:c.*133+246_*133+249dup	ENSP00000431637.1:n.*133+246_*133+249dup
ENST00000487921.5:n.617+246_617+249dup
ENST00000583539.5:c.705+246_705+249dup	ENSP00000463121.1:n.705+246_705+249dup
ENST00000584617.5:c.427+246_427+249dup
NM_058216.2:c.705+246_705+249dup	NP_478123.1:n.705+246_705+249dup
NR_103872.1:n.609+246_609+249dup
XM_006722001.2:c.705+246_705+249dup	XP_006722064.1:n.705+246_705+249dup
XM_006722002.2:c.705+246_705+249dup	XP_006722065.1:n.705+246_705+249dup
XM_006722004.2:c.354+246_354+249dup	XP_006722067.1:n.354+246_354+249dup
XM_006722005.2:c.354+246_354+249dup	XP_006722068.1:n.354+246_354+249dup
XM_011525092.1:c.354+246_354+249dup	XP_011523394.1:n.354+246_354+249dup
XM_011525093.1:c.354+246_354+249dup	XP_011523395.1:n.354+246_354+249dup
XM_011525094.1:c.354+246_354+249dup	XP_011523396.1:n.354+246_354+249dup
XR_934513.1:n.778+246_778+249dup
XR_934514.1:n.778+246_778+249dup
XM_006722001.4:c.705+246_705+249dup	XP_006722064.1:n.705+246_705+249dup
XM_006722002.4:c.705+246_705+249dup	XP_006722065.1:n.705+246_705+249dup
XM_006722004.3:c.354+246_354+249dup	XP_006722067.1:n.354+246_354+249dup
XM_006722005.3:c.354+246_354+249dup	XP_006722068.1:n.354+246_354+249dup
XM_011525092.2:c.354+246_354+249dup	XP_011523394.1:n.354+246_354+249dup
XM_011525093.2:c.354+246_354+249dup	XP_011523395.1:n.354+246_354+249dup
XM_011525094.2:c.354+246_354+249dup	XP_011523396.1:n.354+246_354+249dup
XM_017024914.1:c.354+246_354+249dup	XP_016880403.1:n.354+246_354+249dup
XM_017024915.1:c.354+246_354+249dup	XP_016880404.1:n.354+246_354+249dup
XM_017024916.1:c.354+246_354+249dup	XP_016880405.1:n.354+246_354+249dup
XM_017024917.1:c.354+246_354+249dup	XP_016880406.1:n.354+246_354+249dup
XM_017024918.2:c.354+246_354+249dup	XP_016880407.1:n.354+246_354+249dup
XM_017024919.1:c.354+246_354+249dup	XP_016880408.1:n.354+246_354+249dup
XR_934513.3:n.1209+246_1209+249dup
XR_934514.3:n.1209+246_1209+249dup
NM_058216.3:c.705+246_705+249dup MANE Select	NP_478123.1:n.705+246_705+249dup
NR_103872.2:n.580+246_580+249dup