Canonical Allele Identifier: CA3060596533

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692805_58692806del , CM000679.2:g.58692805_58692806del	GRCh38
NC_000017.10:g.56770166_56770167del , CM000679.1:g.56770166_56770167del	GRCh37
NC_000017.9:g.54125165_54125166del	NCBI36
NG_023199.1:g.5204_5205del , LRG_314:g.5204_5205del
NG_047169.1:g.4274_4275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+120_-207+121del	ENSP00000464056.2:n.-207+120_-207+121del
ENST00000697675.1:n.233_234del
ENST00000697676.1:n.205+17_205+18del
ENST00000697677.1:n.220_221del
ENST00000697678.1:n.47+173_47+174del
ENST00000697679.1:n.213_214del
ENST00000697680.1:c.*3_*4del	ENSP00000513392.1:n.*3_*4del
ENST00000697681.1:c.*3_*4del	ENSP00000513393.1:n.*3_*4del
ENST00000697683.1:c.*3_*4del	ENSP00000513395.1:n.*3_*4del
ENST00000697684.1:n.205+17_205+18del
ENST00000697685.1:c.*3_*4del	ENSP00000513396.1:n.*3_*4del
ENST00000697686.1:c.-207+173_-207+174del	ENSP00000513397.1:n.-207+173_-207+174del
ENST00000697687.1:n.191+17_191+18del
ENST00000697688.1:n.191+17_191+18del
ENST00000697689.1:c.*3_*4del	ENSP00000513398.1:n.*3_*4del
ENST00000697690.1:c.145+17_145+18del	ENSP00000513399.1:n.145+17_145+18del
ENST00000697691.1:c.42+120_42+121del	ENSP00000513400.1:n.42+120_42+121del
ENST00000697692.1:c.*3_*4del	ENSP00000513401.1:n.*3_*4del
ENST00000697693.1:n.75_76del
ENST00000337432.9:c.145+17_145+18del MANE Select	ENSP00000336701.4:n.145+17_145+18del
ENST00000337432.8:c.145+17_145+18del	ENSP00000336701.4:n.145+17_145+18del
ENST00000421782.3:c.145+17_145+18del	ENSP00000391450.2:n.145+17_145+18del
ENST00000461271.5:c.-207+120_-207+121del	ENSP00000464056.1:n.-207+120_-207+121del
ENST00000475762.5:c.*3_*4del	ENSP00000432421.1:n.*3_*4del
ENST00000476741.2:n.187+17_187+18del
ENST00000482007.5:c.145+17_145+18del	ENSP00000433332.1:n.145+17_145+18del
ENST00000486827.1:c.*3_*4del	ENSP00000436761.1:n.*3_*4del
ENST00000487525.5:c.145+17_145+18del	ENSP00000431637.1:n.145+17_145+18del
ENST00000487921.5:n.57+173_57+174del
ENST00000583539.5:c.145+17_145+18del	ENSP00000463121.1:n.145+17_145+18del
ENST00000584617.5:c.126+17_126+18del
NM_002876.3:c.145+17_145+18del	NP_002867.1:n.145+17_145+18del
NM_058216.2:c.145+17_145+18del	NP_478123.1:n.145+17_145+18del
NR_103872.1:n.216+17_216+18del
NR_103873.1:n.113+120_113+121del
XM_006722001.2:c.145+17_145+18del	XP_006722064.1:n.145+17_145+18del
XM_006722002.2:c.145+17_145+18del	XP_006722065.1:n.145+17_145+18del
XM_006722004.2:c.-207+120_-207+121del	XP_006722067.1:n.-207+120_-207+121del
XM_006722005.2:c.-207+173_-207+174del	XP_006722068.1:n.-207+173_-207+174del
XM_011525092.1:c.-507+120_-507+121del	XP_011523394.1:n.-507+120_-507+121del
XM_011525093.1:c.-668+120_-668+121del	XP_011523395.1:n.-668+120_-668+121del
XM_011525094.1:c.-361_-360del	XP_011523396.1:n.-361_-360del
XR_934513.1:n.218+17_218+18del
XR_934514.1:n.218+17_218+18del
XM_006722001.4:c.145+17_145+18del	XP_006722064.1:n.145+17_145+18del
XM_006722002.4:c.145+17_145+18del	XP_006722065.1:n.145+17_145+18del
XM_006722004.3:c.-207+120_-207+121del	XP_006722067.1:n.-207+120_-207+121del
XM_006722005.3:c.-207+173_-207+174del	XP_006722068.1:n.-207+173_-207+174del
XM_011525092.2:c.-507+120_-507+121del	XP_011523394.1:n.-507+120_-507+121del
XM_011525093.2:c.-668+120_-668+121del	XP_011523395.1:n.-668+120_-668+121del
XM_011525094.2:c.-361_-360del	XP_011523396.1:n.-361_-360del
XM_017024914.1:c.-207+120_-207+121del	XP_016880403.1:n.-207+120_-207+121del
XM_017024916.1:c.-507+120_-507+121del	XP_016880405.1:n.-507+120_-507+121del
XM_017024917.1:c.-207+173_-207+174del	XP_016880406.1:n.-207+173_-207+174del
XM_017024918.2:c.-361_-360del	XP_016880407.1:n.-361_-360del
XM_017024919.1:c.-668+120_-668+121del	XP_016880408.1:n.-668+120_-668+121del
XR_934513.3:n.649+17_649+18del
XR_934514.3:n.649+17_649+18del
NM_058216.3:c.145+17_145+18del MANE Select	NP_478123.1:n.145+17_145+18del
NR_103872.2:n.187+17_187+18del
NM_002876.4:c.145+17_145+18del	NP_002867.1:n.145+17_145+18del