Canonical Allele Identifier: CA2267814323

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58693152_58693153delinsTG , CM000679.2:g.58693152_58693153delinsTG	GRCh38
NC_000017.10:g.56770513_56770514delinsTG , CM000679.1:g.56770513_56770514delinsTG	GRCh37
NC_000017.9:g.54125512_54125513delinsTG	NCBI36
NG_023199.1:g.5551_5552delinsTG , LRG_314:g.5551_5552delinsTG
NG_047169.1:g.3927_3928delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+467_-207+468delinsTG	ENSP00000464056.2:n.-207+467_-207+468delinsTG
ENST00000697675.1:n.580_581delinsTG
ENST00000697676.1:n.205+364_205+365delinsTG
ENST00000697677.1:n.567_568delinsTG
ENST00000697678.1:n.47+520_47+521delinsTG
ENST00000697679.1:n.560_561delinsTG
ENST00000697680.1:c.*350_*351delinsTG	ENSP00000513392.1:n.*350_*351delinsTG
ENST00000697681.1:c.*350_*351delinsTG	ENSP00000513393.1:n.*350_*351delinsTG
ENST00000697683.1:c.*350_*351delinsTG	ENSP00000513395.1:n.*350_*351delinsTG
ENST00000697684.1:n.205+364_205+365delinsTG
ENST00000697685.1:c.*350_*351delinsTG	ENSP00000513396.1:n.*350_*351delinsTG
ENST00000697686.1:c.-207+520_-207+521delinsTG	ENSP00000513397.1:n.-207+520_-207+521delinsTG
ENST00000697687.1:n.191+364_191+365delinsTG
ENST00000697688.1:n.191+364_191+365delinsTG
ENST00000697689.1:c.*350_*351delinsTG	ENSP00000513398.1:n.*350_*351delinsTG
ENST00000697690.1:c.145+364_145+365delinsTG	ENSP00000513399.1:n.145+364_145+365delinsTG
ENST00000697691.1:c.43-199_43-198delinsTG	ENSP00000513400.1:n.43-199_43-198delinsTG
ENST00000697692.1:c.*157+193_*157+194delinsTG	ENSP00000513401.1:n.*157+193_*157+194delinsTG
ENST00000697693.1:n.422_423delinsTG
ENST00000697694.1:c.-207+34_-207+35delinsTG	ENSP00000513402.1:n.-207+34_-207+35delinsTG
ENST00000697695.1:n.226_227delinsTG
ENST00000337432.9:c.145+364_145+365delinsTG MANE Select	ENSP00000336701.4:n.145+364_145+365delinsTG
ENST00000337432.8:c.145+364_145+365delinsTG	ENSP00000336701.4:n.145+364_145+365delinsTG
ENST00000421782.3:c.145+364_145+365delinsTG	ENSP00000391450.2:n.145+364_145+365delinsTG
ENST00000461271.5:c.-207+467_-207+468delinsTG	ENSP00000464056.1:n.-207+467_-207+468delinsTG
ENST00000475762.5:c.*350_*351delinsTG	ENSP00000432421.1:n.*350_*351delinsTG
ENST00000476741.2:n.188-199_188-198delinsTG
ENST00000482007.5:c.145+364_145+365delinsTG	ENSP00000433332.1:n.145+364_145+365delinsTG
ENST00000486827.1:c.*350_*351delinsTG	ENSP00000436761.1:n.*350_*351delinsTG
ENST00000487525.5:c.145+364_145+365delinsTG	ENSP00000431637.1:n.145+364_145+365delinsTG
ENST00000487921.5:n.57+520_57+521delinsTG
ENST00000583539.5:c.145+364_145+365delinsTG	ENSP00000463121.1:n.145+364_145+365delinsTG
ENST00000584617.5:c.126+364_126+365delinsTG
NM_002876.3:c.145+364_145+365delinsTG	NP_002867.1:n.145+364_145+365delinsTG
NM_058216.2:c.145+364_145+365delinsTG	NP_478123.1:n.145+364_145+365delinsTG
NR_103872.1:n.216+364_216+365delinsTG
NR_103873.1:n.113+467_113+468delinsTG
XM_006722001.2:c.145+364_145+365delinsTG	XP_006722064.1:n.145+364_145+365delinsTG
XM_006722002.2:c.145+364_145+365delinsTG	XP_006722065.1:n.145+364_145+365delinsTG
XM_006722004.2:c.-207+467_-207+468delinsTG	XP_006722067.1:n.-207+467_-207+468delinsTG
XM_006722005.2:c.-207+520_-207+521delinsTG	XP_006722068.1:n.-207+520_-207+521delinsTG
XM_011525092.1:c.-506-199_-506-198delinsTG	XP_011523394.1:n.-506-199_-506-198delinsTG
XM_011525093.1:c.-667-199_-667-198delinsTG	XP_011523395.1:n.-667-199_-667-198delinsTG
XM_011525094.1:c.-207+193_-207+194delinsTG	XP_011523396.1:n.-207+193_-207+194delinsTG
XR_934513.1:n.218+364_218+365delinsTG
XR_934514.1:n.218+364_218+365delinsTG
XM_006722001.4:c.145+364_145+365delinsTG	XP_006722064.1:n.145+364_145+365delinsTG
XM_006722002.4:c.145+364_145+365delinsTG	XP_006722065.1:n.145+364_145+365delinsTG
XM_006722004.3:c.-207+467_-207+468delinsTG	XP_006722067.1:n.-207+467_-207+468delinsTG
XM_006722005.3:c.-207+520_-207+521delinsTG	XP_006722068.1:n.-207+520_-207+521delinsTG
XM_011525092.2:c.-506-199_-506-198delinsTG	XP_011523394.1:n.-506-199_-506-198delinsTG
XM_011525093.2:c.-667-199_-667-198delinsTG	XP_011523395.1:n.-667-199_-667-198delinsTG
XM_011525094.2:c.-207+193_-207+194delinsTG	XP_011523396.1:n.-207+193_-207+194delinsTG
XM_017024914.1:c.-207+467_-207+468delinsTG	XP_016880403.1:n.-207+467_-207+468delinsTG
XM_017024916.1:c.-506-199_-506-198delinsTG	XP_016880405.1:n.-506-199_-506-198delinsTG
XM_017024917.1:c.-207+520_-207+521delinsTG	XP_016880406.1:n.-207+520_-207+521delinsTG
XM_017024918.2:c.-207+193_-207+194delinsTG	XP_016880407.1:n.-207+193_-207+194delinsTG
XM_017024919.1:c.-667-199_-667-198delinsTG	XP_016880408.1:n.-667-199_-667-198delinsTG
XR_934513.3:n.649+364_649+365delinsTG
XR_934514.3:n.649+364_649+365delinsTG
NM_058216.3:c.145+364_145+365delinsTG MANE Select	NP_478123.1:n.145+364_145+365delinsTG
NR_103872.2:n.187+364_187+365delinsTG
NM_002876.4:c.145+364_145+365delinsTG	NP_002867.1:n.145+364_145+365delinsTG