Canonical Allele Identifier: CA10587275

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 262303
• ClinVar RCV Id: RCV000241800
• dbSNP Id: rs886038710
• gnomAD v2: 17-56787162-TTTA-T
• gnomAD v3: 17-58709801-TTTA-T
• gnomAD v4: 17-58709801-TTTA-T
• MyVariant Identifiers: chr17:g.56787174_56787176del (hg19) ; chr17:g.56787163_56787165del (hg19) ; chr17:g.58709813_58709815del (hg38) ; chr17:g.58709802_58709804del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709813_58709815del , CM000679.2:g.58709813_58709815del	GRCh38
NC_000017.10:g.56787174_56787176del , CM000679.1:g.56787174_56787176del	GRCh37
NC_000017.9:g.54142173_54142175del	NCBI36
NG_023199.1:g.22212_22214del , LRG_314:g.22212_22214del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.355-46_355-44del	ENSP00000464056.2:n.355-46_355-44del
ENST00000697678.1:n.608-46_608-44del
ENST00000697679.1:n.1780-46_1780-44del
ENST00000697680.1:c.*1570-46_*1570-44del	ENSP00000513392.1:n.*1570-46_*1570-44del
ENST00000697681.1:c.*1867-46_*1867-44del	ENSP00000513393.1:n.*1867-46_*1867-44del
ENST00000697683.1:c.*1570-46_*1570-44del	ENSP00000513395.1:n.*1570-46_*1570-44del
ENST00000697684.1:n.766-46_766-44del
ENST00000697685.1:c.*1403-46_*1403-44del	ENSP00000513396.1:n.*1403-46_*1403-44del
ENST00000697686.1:c.355-46_355-44del	ENSP00000513397.1:n.355-46_355-44del
ENST00000697687.1:n.585-46_585-44del
ENST00000697688.1:n.752-46_752-44del
ENST00000697689.1:c.*1242-46_*1242-44del	ENSP00000513398.1:n.*1242-46_*1242-44del
ENST00000697690.1:c.706-46_706-44del	ENSP00000513399.1:n.706-46_706-44del
ENST00000697691.1:c.*678-46_*678-44del	ENSP00000513400.1:n.*678-46_*678-44del
ENST00000697692.1:c.*718-46_*718-44del	ENSP00000513401.1:n.*718-46_*718-44del
ENST00000697694.1:c.355-46_355-44del	ENSP00000513402.1:n.355-46_355-44del
ENST00000697695.1:n.1313-46_1313-44del
ENST00000337432.9:c.706-46_706-44del MANE Select	ENSP00000336701.4:n.706-46_706-44del
ENST00000337432.8:c.706-46_706-44del	ENSP00000336701.4:n.706-46_706-44del
ENST00000413590.5:c.344-46_344-44del
ENST00000425173.5:c.622-46_622-44del	ENSP00000407282.1:n.622-46_622-44del
ENST00000461271.5:c.355-46_355-44del	ENSP00000464056.1:n.355-46_355-44del
ENST00000475762.5:c.*1409-46_*1409-44del	ENSP00000432421.1:n.*1409-46_*1409-44del
ENST00000482007.5:c.*134-46_*134-44del	ENSP00000433332.1:n.*134-46_*134-44del
ENST00000487525.5:c.*279-46_*279-44del	ENSP00000431637.1:n.*279-46_*279-44del
ENST00000581221.5:n.175_177del
ENST00000583539.5:c.706-46_706-44del	ENSP00000463121.1:n.706-46_706-44del
ENST00000584617.5:c.428-46_428-44del
NM_058216.2:c.706-46_706-44del	NP_478123.1:n.706-46_706-44del
NR_103872.1:n.610-46_610-44del
XM_006722001.2:c.706-46_706-44del	XP_006722064.1:n.706-46_706-44del
XM_006722002.2:c.706-46_706-44del	XP_006722065.1:n.706-46_706-44del
XM_006722004.2:c.355-46_355-44del	XP_006722067.1:n.355-46_355-44del
XM_006722005.2:c.355-46_355-44del	XP_006722068.1:n.355-46_355-44del
XM_011525092.1:c.355-46_355-44del	XP_011523394.1:n.355-46_355-44del
XM_011525093.1:c.355-46_355-44del	XP_011523395.1:n.355-46_355-44del
XM_011525094.1:c.355-46_355-44del	XP_011523396.1:n.355-46_355-44del
XR_934513.1:n.924-46_924-44del
XR_934514.1:n.924-46_924-44del
XM_006722001.4:c.706-46_706-44del	XP_006722064.1:n.706-46_706-44del
XM_006722002.4:c.706-46_706-44del	XP_006722065.1:n.706-46_706-44del
XM_006722004.3:c.355-46_355-44del	XP_006722067.1:n.355-46_355-44del
XM_006722005.3:c.355-46_355-44del	XP_006722068.1:n.355-46_355-44del
XM_011525092.2:c.355-46_355-44del	XP_011523394.1:n.355-46_355-44del
XM_011525093.2:c.355-46_355-44del	XP_011523395.1:n.355-46_355-44del
XM_011525094.2:c.355-46_355-44del	XP_011523396.1:n.355-46_355-44del
XM_017024914.1:c.355-46_355-44del	XP_016880403.1:n.355-46_355-44del
XM_017024915.1:c.355-46_355-44del	XP_016880404.1:n.355-46_355-44del
XM_017024916.1:c.355-46_355-44del	XP_016880405.1:n.355-46_355-44del
XM_017024917.1:c.355-46_355-44del	XP_016880406.1:n.355-46_355-44del
XM_017024918.2:c.355-46_355-44del	XP_016880407.1:n.355-46_355-44del
XM_017024919.1:c.355-46_355-44del	XP_016880408.1:n.355-46_355-44del
XR_934513.3:n.1355-46_1355-44del
XR_934514.3:n.1355-46_1355-44del
NM_058216.3:c.706-46_706-44del MANE Select	NP_478123.1:n.706-46_706-44del
NR_103872.2:n.581-46_581-44del