Canonical Allele Identifier: CA2573054504

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1098890
• ClinVar RCV Id: RCV001779190
• dbSNP Id: rs2143670048

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692631_58692657del , CM000679.2:g.58692631_58692657del	GRCh38
NC_000017.10:g.56769992_56770018del , CM000679.1:g.56769992_56770018del	GRCh37
NC_000017.9:g.54124991_54125017del	NCBI36
NG_023199.1:g.5030_5056del , LRG_314:g.5030_5056del
NG_047169.1:g.4424_4450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-261_-235del	ENSP00000464056.2:n.-261_-235del
ENST00000697675.1:n.59_85del
ENST00000697676.1:n.48_74del
ENST00000697677.1:n.46_72del
ENST00000697678.1:n.46_47+25del
ENST00000697679.1:n.39_65del
ENST00000697680.1:c.-13_14del
ENST00000697681.1:c.-13_14del
ENST00000697683.1:c.-13_14del
ENST00000697684.1:n.48_74del
ENST00000697685.1:c.-13_14del
ENST00000697686.1:c.-208_-207+25del
ENST00000697687.1:n.34_60del
ENST00000697688.1:n.34_60del
ENST00000697689.1:c.-13_14del
ENST00000697690.1:c.-13_14del
ENST00000697691.1:c.-13_14del
ENST00000337432.9:c.-13_14del
ENST00000337432.8:c.-13_14del
ENST00000421782.3:c.-13_14del
ENST00000461271.5:c.-261_-235del	ENSP00000464056.1:n.-261_-235del
ENST00000475762.5:c.-13_14del
ENST00000476741.2:n.30_56del
ENST00000482007.5:c.-13_14del
ENST00000486827.1:c.-13_14del
ENST00000487525.5:c.-13_14del
ENST00000487921.5:n.56_57+25del
ENST00000583539.5:c.-13_14del
NM_002876.3:c.-13_14del
NM_058216.2:c.-13_14del
NR_103872.1:n.59_85del
NR_103873.1:n.59_85del
XM_006722001.2:c.-13_14del
XM_006722002.2:c.-13_14del
XM_006722004.2:c.-261_-235del	XP_006722067.1:n.-261_-235del
XM_006722005.2:c.-208_-207+25del
XM_011525092.1:c.-561_-535del	XP_011523394.1:n.-561_-535del
XM_011525093.1:c.-722_-696del	XP_011523395.1:n.-722_-696del
XR_934513.1:n.61_87del
XR_934514.1:n.61_87del
XM_006722001.4:c.-13_14del
XM_006722002.4:c.-13_14del
XM_006722004.3:c.-261_-235del	XP_006722067.1:n.-261_-235del
XM_006722005.3:c.-208_-207+25del
XM_017024914.1:c.-261_-235del	XP_016880403.1:n.-261_-235del
XM_017024916.1:c.-561_-535del	XP_016880405.1:n.-561_-535del
XM_017024917.1:c.-208_-207+25del
XR_934513.3:n.492_518del
XR_934514.3:n.492_518del
NM_058216.3:c.-13_14del
NR_103872.2:n.30_56del
NM_002876.4:c.-13_14del