Canonical Allele Identifier: CA3057227955

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692640_58692642del , CM000679.2:g.58692640_58692642del	GRCh38
NC_000017.10:g.56770001_56770003del , CM000679.1:g.56770001_56770003del	GRCh37
NC_000017.9:g.54125000_54125002del	NCBI36
NG_023199.1:g.5039_5041del , LRG_314:g.5039_5041del
NG_047169.1:g.4439_4441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-252_-250del	ENSP00000464056.2:n.-252_-250del
ENST00000697675.1:n.68_70del
ENST00000697676.1:n.57_59del
ENST00000697677.1:n.55_57del
ENST00000697678.1:n.47+8_47+10del
ENST00000697679.1:n.48_50del
ENST00000697680.1:c.-4_-2del	ENSP00000513392.1:n.-4_-2del
ENST00000697681.1:c.-4_-2del	ENSP00000513393.1:n.-4_-2del
ENST00000697683.1:c.-4_-2del	ENSP00000513395.1:n.-4_-2del
ENST00000697684.1:n.57_59del
ENST00000697685.1:c.-4_-2del	ENSP00000513396.1:n.-4_-2del
ENST00000697686.1:c.-207+8_-207+10del	ENSP00000513397.1:n.-207+8_-207+10del
ENST00000697687.1:n.43_45del
ENST00000697688.1:n.43_45del
ENST00000697689.1:c.-4_-2del	ENSP00000513398.1:n.-4_-2del
ENST00000697690.1:c.-4_-2del	ENSP00000513399.1:n.-4_-2del
ENST00000697691.1:c.-4_-2del	ENSP00000513400.1:n.-4_-2del
ENST00000697692.1:c.-4_-2del	ENSP00000513401.1:n.-4_-2del
ENST00000337432.9:c.-4_-2del MANE Select	ENSP00000336701.4:n.-4_-2del
ENST00000337432.8:c.-4_-2del	ENSP00000336701.4:n.-4_-2del
ENST00000421782.3:c.-4_-2del	ENSP00000391450.2:n.-4_-2del
ENST00000461271.5:c.-252_-250del	ENSP00000464056.1:n.-252_-250del
ENST00000475762.5:c.-4_-2del	ENSP00000432421.1:n.-4_-2del
ENST00000476741.2:n.39_41del
ENST00000482007.5:c.-4_-2del	ENSP00000433332.1:n.-4_-2del
ENST00000486827.1:c.-4_-2del	ENSP00000436761.1:n.-4_-2del
ENST00000487525.5:c.-4_-2del	ENSP00000431637.1:n.-4_-2del
ENST00000487921.5:n.57+8_57+10del
ENST00000583539.5:c.-4_-2del	ENSP00000463121.1:n.-4_-2del
NM_002876.3:c.-4_-2del	NP_002867.1:n.-4_-2del
NM_058216.2:c.-4_-2del	NP_478123.1:n.-4_-2del
NR_103872.1:n.68_70del
NR_103873.1:n.68_70del
XM_006722001.2:c.-4_-2del	XP_006722064.1:n.-4_-2del
XM_006722002.2:c.-4_-2del	XP_006722065.1:n.-4_-2del
XM_006722004.2:c.-252_-250del	XP_006722067.1:n.-252_-250del
XM_006722005.2:c.-207+8_-207+10del	XP_006722068.1:n.-207+8_-207+10del
XM_011525092.1:c.-552_-550del	XP_011523394.1:n.-552_-550del
XM_011525093.1:c.-713_-711del	XP_011523395.1:n.-713_-711del
XR_934513.1:n.70_72del
XR_934514.1:n.70_72del
XM_006722001.4:c.-4_-2del	XP_006722064.1:n.-4_-2del
XM_006722002.4:c.-4_-2del	XP_006722065.1:n.-4_-2del
XM_006722004.3:c.-252_-250del	XP_006722067.1:n.-252_-250del
XM_006722005.3:c.-207+8_-207+10del	XP_006722068.1:n.-207+8_-207+10del
XM_017024914.1:c.-252_-250del	XP_016880403.1:n.-252_-250del
XM_017024916.1:c.-552_-550del	XP_016880405.1:n.-552_-550del
XM_017024917.1:c.-207+8_-207+10del	XP_016880406.1:n.-207+8_-207+10del
XM_017024918.2:c.-526_-524del	XP_016880407.1:n.-526_-524del
XR_934513.3:n.501_503del
XR_934514.3:n.501_503del
NM_058216.3:c.-4_-2del MANE Select	NP_478123.1:n.-4_-2del
NR_103872.2:n.39_41del
NM_002876.4:c.-4_-2del	NP_002867.1:n.-4_-2del