Canonical Allele Identifier: CA2639016901

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58724201-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724201_58724202insC , CM000679.2:g.58724201_58724202insC	GRCh38
NC_000017.10:g.56801562_56801563insC , CM000679.1:g.56801562_56801563insC	GRCh37
NC_000017.9:g.54156561_54156562insC	NCBI36
NG_023199.1:g.36600_36601insC , LRG_314:g.36600_36601insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.614+101_614+102insC	ENSP00000464056.2:n.614+101_614+102insC
ENST00000697680.1:c.*1929+101_*1929+102insC	ENSP00000513392.1:n.*1929+101_*1929+102insC
ENST00000697681.1:c.*2126+101_*2126+102insC	ENSP00000513393.1:n.*2126+101_*2126+102insC
ENST00000697683.1:c.*1829+101_*1829+102insC	ENSP00000513395.1:n.*1829+101_*1829+102insC
ENST00000697684.1:n.1025+101_1025+102insC
ENST00000697685.1:c.*1662+101_*1662+102insC	ENSP00000513396.1:n.*1662+101_*1662+102insC
ENST00000697686.1:c.614+101_614+102insC	ENSP00000513397.1:n.614+101_614+102insC
ENST00000697687.1:n.945_946insC
ENST00000697688.1:n.1112_1113insC
ENST00000697689.1:c.*1440+3389_*1440+3390insC	ENSP00000513398.1:n.*1440+3389_*1440+3390insC
ENST00000697690.1:c.904+3389_904+3390insC	ENSP00000513399.1:n.904+3389_904+3390insC
ENST00000697691.1:c.*937+101_*937+102insC	ENSP00000513400.1:n.*937+101_*937+102insC
ENST00000697692.1:c.*977+101_*977+102insC	ENSP00000513401.1:n.*977+101_*977+102insC
ENST00000697694.1:c.614+101_614+102insC	ENSP00000513402.1:n.614+101_614+102insC
ENST00000697695.1:n.1572+101_1572+102insC
ENST00000337432.9:c.965+101_965+102insC MANE Select	ENSP00000336701.4:n.965+101_965+102insC
ENST00000337432.8:c.965+101_965+102insC	ENSP00000336701.4:n.965+101_965+102insC
ENST00000413590.5:c.603+101_603+102insC
ENST00000475762.5:c.*1601+101_*1601+102insC	ENSP00000432421.1:n.*1601+101_*1601+102insC
ENST00000482007.5:c.*393+101_*393+102insC	ENSP00000433332.1:n.*393+101_*393+102insC
ENST00000487525.5:c.*538+101_*538+102insC	ENSP00000431637.1:n.*538+101_*538+102insC
ENST00000578151.1:n.239+3389_239+3390insC
ENST00000581221.5:n.480+101_480+102insC
ENST00000583539.5:c.965+101_965+102insC	ENSP00000463121.1:n.965+101_965+102insC
ENST00000584617.5:c.687+101_687+102insC
ENST00000584804.1:c.199+3389_199+3390insC	ENSP00000463658.1:n.199+3389_199+3390insC
NM_058216.2:c.965+101_965+102insC	NP_478123.1:n.965+101_965+102insC
NR_103872.1:n.869+101_869+102insC
XM_006722001.2:c.965+101_965+102insC	XP_006722064.1:n.965+101_965+102insC
XM_006722002.2:c.904+3389_904+3390insC	XP_006722065.1:n.904+3389_904+3390insC
XM_006722004.2:c.614+101_614+102insC	XP_006722067.1:n.614+101_614+102insC
XM_006722005.2:c.614+101_614+102insC	XP_006722068.1:n.614+101_614+102insC
XM_011525092.1:c.614+101_614+102insC	XP_011523394.1:n.614+101_614+102insC
XM_011525093.1:c.614+101_614+102insC	XP_011523395.1:n.614+101_614+102insC
XM_011525094.1:c.614+101_614+102insC	XP_011523396.1:n.614+101_614+102insC
XR_934513.1:n.1183+101_1183+102insC
XR_934514.1:n.1183+101_1183+102insC
XR_934886.1:n.373_374insG
XM_006722001.4:c.965+101_965+102insC	XP_006722064.1:n.965+101_965+102insC
XM_006722002.4:c.904+3389_904+3390insC	XP_006722065.1:n.904+3389_904+3390insC
XM_006722004.3:c.614+101_614+102insC	XP_006722067.1:n.614+101_614+102insC
XM_006722005.3:c.614+101_614+102insC	XP_006722068.1:n.614+101_614+102insC
XM_011525092.2:c.614+101_614+102insC	XP_011523394.1:n.614+101_614+102insC
XM_011525093.2:c.614+101_614+102insC	XP_011523395.1:n.614+101_614+102insC
XM_011525094.2:c.614+101_614+102insC	XP_011523396.1:n.614+101_614+102insC
XM_017024914.1:c.614+101_614+102insC	XP_016880403.1:n.614+101_614+102insC
XM_017024915.1:c.614+101_614+102insC	XP_016880404.1:n.614+101_614+102insC
XM_017024916.1:c.614+101_614+102insC	XP_016880405.1:n.614+101_614+102insC
XM_017024917.1:c.614+101_614+102insC	XP_016880406.1:n.614+101_614+102insC
XM_017024918.2:c.614+101_614+102insC	XP_016880407.1:n.614+101_614+102insC
XM_017024919.1:c.553+3389_553+3390insC	XP_016880408.1:n.553+3389_553+3390insC
XR_934513.3:n.1614+101_1614+102insC
XR_934514.3:n.1614+101_1614+102insC
XR_934886.2:n.373_374insG
NM_058216.3:c.965+101_965+102insC MANE Select	NP_478123.1:n.965+101_965+102insC
NR_103872.2:n.840+101_840+102insC