Canonical Allele Identifier: CA2639015943

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58703247-TTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703253_58703255del , CM000679.2:g.58703253_58703255del	GRCh38
NC_000017.10:g.56780614_56780616del , CM000679.1:g.56780614_56780616del	GRCh37
NC_000017.9:g.54135613_54135615del	NCBI36
NG_023199.1:g.15652_15654del , LRG_314:g.15652_15654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.278_280del	ENSP00000464056.2:p.Tyr93del
ENST00000697677.1:n.1710_1712del
ENST00000697678.1:n.531_533del
ENST00000697679.1:n.1703_1705del
ENST00000697680.1:c.*1493_*1495del	ENSP00000513392.1:n.*1493_*1495del
ENST00000697681.1:c.*1645_*1647del	ENSP00000513393.1:n.*1645_*1647del
ENST00000697683.1:c.*1493_*1495del	ENSP00000513395.1:n.*1493_*1495del
ENST00000697684.1:n.689_691del
ENST00000697685.1:c.*1326_*1328del	ENSP00000513396.1:n.*1326_*1328del
ENST00000697686.1:c.278_280del	ENSP00000513397.1:p.Tyr93del
ENST00000697687.1:n.508_510del
ENST00000697688.1:n.675_677del
ENST00000697689.1:c.*1165_*1167del	ENSP00000513398.1:n.*1165_*1167del
ENST00000697690.1:c.629_631del	ENSP00000513399.1:p.Tyr210del
ENST00000697691.1:c.*601_*603del	ENSP00000513400.1:n.*601_*603del
ENST00000697692.1:c.*641_*643del	ENSP00000513401.1:n.*641_*643del
ENST00000697694.1:c.278_280del	ENSP00000513402.1:p.Tyr93del
ENST00000697695.1:n.1236_1238del
ENST00000337432.9:c.629_631del MANE Select	ENSP00000336701.4:p.Tyr210del
ENST00000337432.8:c.629_631del	ENSP00000336701.4:p.Tyr210del
ENST00000413590.5:c.267_269del
ENST00000425173.5:c.425_427del	ENSP00000407282.1:p.Tyr142del
ENST00000461271.5:c.278_280del	ENSP00000464056.1:p.Tyr93del
ENST00000475762.5:c.*1332_*1334del	ENSP00000432421.1:n.*1332_*1334del
ENST00000482007.5:c.*57_*59del	ENSP00000433332.1:n.*57_*59del
ENST00000487525.5:c.*57_*59del	ENSP00000431637.1:n.*57_*59del
ENST00000487921.5:n.541_543del
ENST00000583539.5:c.629_631del	ENSP00000463121.1:p.Tyr210del
ENST00000584617.5:c.351_353del
NM_058216.2:c.629_631del	NP_478123.1:p.Tyr210del
NR_103872.1:n.533_535del
XM_006722001.2:c.629_631del	XP_006722064.1:p.Tyr210del
XM_006722002.2:c.629_631del	XP_006722065.1:p.Tyr210del
XM_006722004.2:c.278_280del	XP_006722067.1:p.Tyr93del
XM_006722005.2:c.278_280del	XP_006722068.1:p.Tyr93del
XM_011525092.1:c.278_280del	XP_011523394.1:p.Tyr93del
XM_011525093.1:c.278_280del	XP_011523395.1:p.Tyr93del
XM_011525094.1:c.278_280del	XP_011523396.1:p.Tyr93del
XR_934513.1:n.702_704del
XR_934514.1:n.702_704del
XM_006722001.4:c.629_631del	XP_006722064.1:p.Tyr210del
XM_006722002.4:c.629_631del	XP_006722065.1:p.Tyr210del
XM_006722004.3:c.278_280del	XP_006722067.1:p.Tyr93del
XM_006722005.3:c.278_280del	XP_006722068.1:p.Tyr93del
XM_011525092.2:c.278_280del	XP_011523394.1:p.Tyr93del
XM_011525093.2:c.278_280del	XP_011523395.1:p.Tyr93del
XM_011525094.2:c.278_280del	XP_011523396.1:p.Tyr93del
XM_017024914.1:c.278_280del	XP_016880403.1:p.Tyr93del
XM_017024915.1:c.278_280del	XP_016880404.1:p.Tyr93del
XM_017024916.1:c.278_280del	XP_016880405.1:p.Tyr93del
XM_017024917.1:c.278_280del	XP_016880406.1:p.Tyr93del
XM_017024918.2:c.278_280del	XP_016880407.1:p.Tyr93del
XM_017024919.1:c.278_280del	XP_016880408.1:p.Tyr93del
XR_934513.3:n.1133_1135del
XR_934514.3:n.1133_1135del
NM_058216.3:c.629_631del MANE Select	NP_478123.1:p.Tyr210del
NR_103872.2:n.504_506del