Canonical Allele Identifier: CA985049613

Gene: RAD51C

Linked Data

• dbSNP Id: rs2047791020
• gnomAD v3: 17-58692602-G-GTGC
• gnomAD v4: 17-58692602-G-GTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692603_58692605dup , CM000679.2:g.58692603_58692605dup	GRCh38
NC_000017.10:g.56769964_56769966dup , CM000679.1:g.56769964_56769966dup	GRCh37
NC_000017.9:g.54124963_54124965dup	NCBI36
NG_023199.1:g.5002_5004dup , LRG_314:g.5002_5004dup
NG_047169.1:g.4475_4477dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-289_-287dup	ENSP00000464056.2:n.-289_-287dup
ENST00000697675.1:n.31_33dup
ENST00000697676.1:n.20_22dup
ENST00000697677.1:n.18_20dup
ENST00000697678.1:n.18_20dup
ENST00000697679.1:n.11_13dup
ENST00000697680.1:c.-41_-39dup	ENSP00000513392.1:n.-41_-39dup
ENST00000697681.1:c.-41_-39dup	ENSP00000513393.1:n.-41_-39dup
ENST00000697683.1:c.-41_-39dup	ENSP00000513395.1:n.-41_-39dup
ENST00000697684.1:n.20_22dup
ENST00000697685.1:c.-41_-39dup	ENSP00000513396.1:n.-41_-39dup
ENST00000697686.1:c.-236_-234dup	ENSP00000513397.1:n.-236_-234dup
ENST00000697687.1:n.6_8dup
ENST00000697688.1:n.6_8dup
ENST00000697689.1:c.-41_-39dup	ENSP00000513398.1:n.-41_-39dup
ENST00000697690.1:c.-41_-39dup	ENSP00000513399.1:n.-41_-39dup
ENST00000337432.9:c.-41_-39dup MANE Select	ENSP00000336701.4:n.-41_-39dup
ENST00000337432.8:c.-41_-39dup	ENSP00000336701.4:n.-41_-39dup
ENST00000461271.5:c.-289_-287dup	ENSP00000464056.1:n.-289_-287dup
ENST00000475762.5:c.-41_-39dup	ENSP00000432421.1:n.-41_-39dup
ENST00000476741.2:n.2_4dup
ENST00000487921.5:n.28_30dup
ENST00000583539.5:c.-41_-39dup	ENSP00000463121.1:n.-41_-39dup
NM_002876.3:c.-41_-39dup	NP_002867.1:n.-41_-39dup
NM_058216.2:c.-41_-39dup	NP_478123.1:n.-41_-39dup
NR_103872.1:n.31_33dup
NR_103873.1:n.31_33dup
XM_006722001.2:c.-41_-39dup	XP_006722064.1:n.-41_-39dup
XM_006722002.2:c.-41_-39dup	XP_006722065.1:n.-41_-39dup
XM_006722004.2:c.-289_-287dup	XP_006722067.1:n.-289_-287dup
XM_006722005.2:c.-236_-234dup	XP_006722068.1:n.-236_-234dup
XM_011525092.1:c.-589_-587dup	XP_011523394.1:n.-589_-587dup
XM_011525093.1:c.-750_-748dup	XP_011523395.1:n.-750_-748dup
XR_934513.1:n.33_35dup
XR_934514.1:n.33_35dup
XM_006722001.4:c.-41_-39dup	XP_006722064.1:n.-41_-39dup
XM_006722002.4:c.-41_-39dup	XP_006722065.1:n.-41_-39dup
XM_006722004.3:c.-289_-287dup	XP_006722067.1:n.-289_-287dup
XM_006722005.3:c.-236_-234dup	XP_006722068.1:n.-236_-234dup
XM_017024914.1:c.-289_-287dup	XP_016880403.1:n.-289_-287dup
XM_017024917.1:c.-236_-234dup	XP_016880406.1:n.-236_-234dup
XR_934513.3:n.464_466dup
XR_934514.3:n.464_466dup
NM_058216.3:c.-41_-39dup MANE Select	NP_478123.1:n.-41_-39dup
NR_103872.2:n.2_4dup
NM_002876.4:c.-41_-39dup	NP_002867.1:n.-41_-39dup