Canonical Allele Identifier: CA10583601

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 241766
• ClinVar RCV Id: RCV000229481
• dbSNP Id: rs878855177
• MyVariant Identifiers: chr17:g.56770151_56770156delinsCTAAG (hg19) ; chr17:g.58692790_58692795delinsCTAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692790_58692795delinsCTAAG , CM000679.2:g.58692790_58692795delinsCTAAG	GRCh38
NC_000017.10:g.56770151_56770156delinsCTAAG , CM000679.1:g.56770151_56770156delinsCTAAG	GRCh37
NC_000017.9:g.54125150_54125155delinsCTAAG	NCBI36
NG_023199.1:g.5189_5194delinsCTAAG , LRG_314:g.5189_5194delinsCTAAG
NG_047169.1:g.4285_4290delinsCTTAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-207+105_-207+110delinsCTAAG	ENSP00000464056.2:n.-207+105_-207+110delinsCTAAG
ENST00000697675.1:n.218_223delinsCTAAG
ENST00000697676.1:n.205+2_205+7delinsCTAAG
ENST00000697677.1:n.205_210delinsCTAAG
ENST00000697678.1:n.47+158_47+163delinsCTAAG
ENST00000697679.1:n.198_203delinsCTAAG
ENST00000697680.1:c.147_152delinsCTAAG	ENSP00000513392.1:p.Asn50Ter
ENST00000697681.1:c.147_152delinsCTAAG	ENSP00000513393.1:p.Asn50Ter
ENST00000697683.1:c.147_152delinsCTAAG	ENSP00000513395.1:p.Asn50Ter
ENST00000697684.1:n.205+2_205+7delinsCTAAG
ENST00000697685.1:c.147_152delinsCTAAG	ENSP00000513396.1:p.Asn50Ter
ENST00000697686.1:c.-207+158_-207+163delinsCTAAG	ENSP00000513397.1:n.-207+158_-207+163delinsCTAAG
ENST00000697687.1:n.191+2_191+7delinsCTAAG
ENST00000697688.1:n.191+2_191+7delinsCTAAG
ENST00000697689.1:c.147_152delinsCTAAG	ENSP00000513398.1:p.Asn50Ter
ENST00000697690.1:c.145+2_145+7delinsCTAAG	ENSP00000513399.1:n.145+2_145+7delinsCTAAG
ENST00000697691.1:c.42+105_42+110delinsCTAAG	ENSP00000513400.1:n.42+105_42+110delinsCTAAG
ENST00000697692.1:c.147_152delinsCTAAG	ENSP00000513401.1:p.Asn50Ter
ENST00000697693.1:n.60_65delinsCTAAG
ENST00000337432.9:c.145+2_145+7delinsCTAAG MANE Select	ENSP00000336701.4:n.145+2_145+7delinsCTAAG
ENST00000337432.8:c.145+2_145+7delinsCTAAG	ENSP00000336701.4:n.145+2_145+7delinsCTAAG
ENST00000421782.3:c.145+2_145+7delinsCTAAG	ENSP00000391450.2:n.145+2_145+7delinsCTAAG
ENST00000461271.5:c.-207+105_-207+110delinsCTAAG	ENSP00000464056.1:n.-207+105_-207+110delinsCTAAG
ENST00000475762.5:c.147_152delinsCTAAG	ENSP00000432421.1:p.Asn50Ter
ENST00000476741.2:n.187+2_187+7delinsCTAAG
ENST00000482007.5:c.145+2_145+7delinsCTAAG	ENSP00000433332.1:n.145+2_145+7delinsCTAAG
ENST00000486827.1:c.147_152delinsCTAAG	ENSP00000436761.1:p.Asn50Ter
ENST00000487525.5:c.145+2_145+7delinsCTAAG	ENSP00000431637.1:n.145+2_145+7delinsCTAAG
ENST00000487921.5:n.57+158_57+163delinsCTAAG
ENST00000583539.5:c.145+2_145+7delinsCTAAG	ENSP00000463121.1:n.145+2_145+7delinsCTAAG
ENST00000584617.5:c.126+2_126+7delinsCTAAG
NM_002876.3:c.145+2_145+7delinsCTAAG	NP_002867.1:n.145+2_145+7delinsCTAAG
NM_058216.2:c.145+2_145+7delinsCTAAG	NP_478123.1:n.145+2_145+7delinsCTAAG
NR_103872.1:n.216+2_216+7delinsCTAAG
NR_103873.1:n.113+105_113+110delinsCTAAG
XM_006722001.2:c.145+2_145+7delinsCTAAG	XP_006722064.1:n.145+2_145+7delinsCTAAG
XM_006722002.2:c.145+2_145+7delinsCTAAG	XP_006722065.1:n.145+2_145+7delinsCTAAG
XM_006722004.2:c.-207+105_-207+110delinsCTAAG	XP_006722067.1:n.-207+105_-207+110delinsCTAAG
XM_006722005.2:c.-207+158_-207+163delinsCTAAG	XP_006722068.1:n.-207+158_-207+163delinsCTAAG
XM_011525092.1:c.-507+105_-507+110delinsCTAAG	XP_011523394.1:n.-507+105_-507+110delinsCTAAG
XM_011525093.1:c.-668+105_-668+110delinsCTAAG	XP_011523395.1:n.-668+105_-668+110delinsCTAAG
XR_934513.1:n.218+2_218+7delinsCTAAG
XR_934514.1:n.218+2_218+7delinsCTAAG
XM_006722001.4:c.145+2_145+7delinsCTAAG	XP_006722064.1:n.145+2_145+7delinsCTAAG
XM_006722002.4:c.145+2_145+7delinsCTAAG	XP_006722065.1:n.145+2_145+7delinsCTAAG
XM_006722004.3:c.-207+105_-207+110delinsCTAAG	XP_006722067.1:n.-207+105_-207+110delinsCTAAG
XM_006722005.3:c.-207+158_-207+163delinsCTAAG	XP_006722068.1:n.-207+158_-207+163delinsCTAAG
XM_011525092.2:c.-507+105_-507+110delinsCTAAG	XP_011523394.1:n.-507+105_-507+110delinsCTAAG
XM_011525093.2:c.-668+105_-668+110delinsCTAAG	XP_011523395.1:n.-668+105_-668+110delinsCTAAG
XM_017024914.1:c.-207+105_-207+110delinsCTAAG	XP_016880403.1:n.-207+105_-207+110delinsCTAAG
XM_017024916.1:c.-507+105_-507+110delinsCTAAG	XP_016880405.1:n.-507+105_-507+110delinsCTAAG
XM_017024917.1:c.-207+158_-207+163delinsCTAAG	XP_016880406.1:n.-207+158_-207+163delinsCTAAG
XM_017024918.2:c.-376_-371delinsCTAAG	XP_016880407.1:n.-376_-371delinsCTAAG
XM_017024919.1:c.-668+105_-668+110delinsCTAAG	XP_016880408.1:n.-668+105_-668+110delinsCTAAG
XR_934513.3:n.649+2_649+7delinsCTAAG
XR_934514.3:n.649+2_649+7delinsCTAAG
NM_058216.3:c.145+2_145+7delinsCTAAG MANE Select	NP_478123.1:n.145+2_145+7delinsCTAAG
NR_103872.2:n.187+2_187+7delinsCTAAG
NM_002876.4:c.145+2_145+7delinsCTAAG	NP_002867.1:n.145+2_145+7delinsCTAAG