Canonical Allele Identifier: CA3057228176

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692707_58692708delinsAA , CM000679.2:g.58692707_58692708delinsAA	GRCh38
NC_000017.10:g.56770068_56770069delinsAA , CM000679.1:g.56770068_56770069delinsAA	GRCh37
NC_000017.9:g.54125067_54125068delinsAA	NCBI36
NG_023199.1:g.5106_5107delinsAA , LRG_314:g.5106_5107delinsAA
NG_047169.1:g.4372_4373delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+22_-207+23delinsAA	ENSP00000464056.2:n.-207+22_-207+23delinsAA
ENST00000697675.1:n.135_136delinsAA
ENST00000697676.1:n.124_125delinsAA
ENST00000697677.1:n.122_123delinsAA
ENST00000697678.1:n.47+75_47+76delinsAA
ENST00000697679.1:n.115_116delinsAA
ENST00000697680.1:c.64_65delinsAA	ENSP00000513392.1:p.Ala22Lys
ENST00000697681.1:c.64_65delinsAA	ENSP00000513393.1:p.Ala22Lys
ENST00000697683.1:c.64_65delinsAA	ENSP00000513395.1:p.Ala22Lys
ENST00000697684.1:n.124_125delinsAA
ENST00000697685.1:c.64_65delinsAA	ENSP00000513396.1:p.Ala22Lys
ENST00000697686.1:c.-207+75_-207+76delinsAA	ENSP00000513397.1:n.-207+75_-207+76delinsAA
ENST00000697687.1:n.110_111delinsAA
ENST00000697688.1:n.110_111delinsAA
ENST00000697689.1:c.64_65delinsAA	ENSP00000513398.1:p.Ala22Lys
ENST00000697690.1:c.64_65delinsAA	ENSP00000513399.1:p.Ala22Lys
ENST00000697691.1:c.42+22_42+23delinsAA	ENSP00000513400.1:n.42+22_42+23delinsAA
ENST00000697692.1:c.64_65delinsAA	ENSP00000513401.1:p.Ala22Lys
ENST00000337432.9:c.64_65delinsAA MANE Select	ENSP00000336701.4:p.Ala22Lys
ENST00000337432.8:c.64_65delinsAA	ENSP00000336701.4:p.Ala22Lys
ENST00000421782.3:c.64_65delinsAA	ENSP00000391450.2:p.Ala22Lys
ENST00000461271.5:c.-207+22_-207+23delinsAA	ENSP00000464056.1:n.-207+22_-207+23delinsAA
ENST00000475762.5:c.64_65delinsAA	ENSP00000432421.1:p.Ala22Lys
ENST00000476741.2:n.106_107delinsAA
ENST00000482007.5:c.64_65delinsAA	ENSP00000433332.1:p.Ala22Lys
ENST00000486827.1:c.64_65delinsAA	ENSP00000436761.1:p.Ala22Lys
ENST00000487525.5:c.64_65delinsAA	ENSP00000431637.1:p.Ala22Lys
ENST00000487921.5:n.57+75_57+76delinsAA
ENST00000583539.5:c.64_65delinsAA	ENSP00000463121.1:p.Ala22Lys
ENST00000584617.5:c.45_46delinsAA
NM_002876.3:c.64_65delinsAA	NP_002867.1:p.Ala22Lys
NM_058216.2:c.64_65delinsAA	NP_478123.1:p.Ala22Lys
NR_103872.1:n.135_136delinsAA
NR_103873.1:n.113+22_113+23delinsAA
XM_006722001.2:c.64_65delinsAA	XP_006722064.1:p.Ala22Lys
XM_006722002.2:c.64_65delinsAA	XP_006722065.1:p.Ala22Lys
XM_006722004.2:c.-207+22_-207+23delinsAA	XP_006722067.1:n.-207+22_-207+23delinsAA
XM_006722005.2:c.-207+75_-207+76delinsAA	XP_006722068.1:n.-207+75_-207+76delinsAA
XM_011525092.1:c.-507+22_-507+23delinsAA	XP_011523394.1:n.-507+22_-507+23delinsAA
XM_011525093.1:c.-668+22_-668+23delinsAA	XP_011523395.1:n.-668+22_-668+23delinsAA
XR_934513.1:n.137_138delinsAA
XR_934514.1:n.137_138delinsAA
XM_006722001.4:c.64_65delinsAA	XP_006722064.1:p.Ala22Lys
XM_006722002.4:c.64_65delinsAA	XP_006722065.1:p.Ala22Lys
XM_006722004.3:c.-207+22_-207+23delinsAA	XP_006722067.1:n.-207+22_-207+23delinsAA
XM_006722005.3:c.-207+75_-207+76delinsAA	XP_006722068.1:n.-207+75_-207+76delinsAA
XM_011525092.2:c.-507+22_-507+23delinsAA	XP_011523394.1:n.-507+22_-507+23delinsAA
XM_011525093.2:c.-668+22_-668+23delinsAA	XP_011523395.1:n.-668+22_-668+23delinsAA
XM_017024914.1:c.-207+22_-207+23delinsAA	XP_016880403.1:n.-207+22_-207+23delinsAA
XM_017024916.1:c.-507+22_-507+23delinsAA	XP_016880405.1:n.-507+22_-507+23delinsAA
XM_017024917.1:c.-207+75_-207+76delinsAA	XP_016880406.1:n.-207+75_-207+76delinsAA
XM_017024918.2:c.-459_-458delinsAA	XP_016880407.1:n.-459_-458delinsAA
XM_017024919.1:c.-668+22_-668+23delinsAA	XP_016880408.1:n.-668+22_-668+23delinsAA
XR_934513.3:n.568_569delinsAA
XR_934514.3:n.568_569delinsAA
NM_058216.3:c.64_65delinsAA MANE Select	NP_478123.1:p.Ala22Lys
NR_103872.2:n.106_107delinsAA
NM_002876.4:c.64_65delinsAA	NP_002867.1:p.Ala22Lys