Canonical Allele Identifier: CA8499756

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 371892
• ClinVar RCV Id: RCV000411057
• dbSNP Id: rs761104531
• ExAC: 17:33446906 ACCTGG / A
• gnomAD v2: 17-33446906-ACCTGG-A
• gnomAD v3: 17-35119887-ACCTGG-A
• gnomAD v4: 17-35119887-ACCTGG-A
• MyVariant Identifiers: chr17:g.33446911_33446915del (hg19) ; chr17:g.33446907_33446911del (hg19) ; chr17:g.35119892_35119896del (hg38) ; chr17:g.35119888_35119892del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35119892_35119896del , CM000679.2:g.35119892_35119896del	GRCh38
NC_000017.10:g.33446911_33446915del , CM000679.1:g.33446911_33446915del	GRCh37
NC_000017.9:g.30471024_30471028del	NCBI36
NG_031858.1:g.4978_4982del , LRG_516:g.4978_4982del
NG_054719.1:g.3314_3318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587405.6:c.-95+1399_-95+1403del	ENSP00000466478.2:n.-95+1399_-95+1403del
ENST00000394589.8:c.-117+130_-117+134del	ENSP00000378090.4:n.-117+130_-117+134del
ENST00000415064.6:n.233-720_233-716del
ENST00000585947.5:n.159+1399_159+1403del
ENST00000585982.5:n.178-720_178-716del
ENST00000587405.5:c.-95+1399_-95+1403del	ENSP00000466478.1:n.-95+1399_-95+1403del
ENST00000587982.5:n.191+1399_191+1403del
ENST00000588372.5:c.-95+1399_-95+1403del	ENSP00000468764.1:n.-95+1399_-95+1403del
ENST00000591723.5:c.-134+1399_-134+1403del	ENSP00000467986.1:n.-134+1399_-134+1403del
ENST00000592181.1:c.-157+155_-157+159del	ENSP00000464799.1:n.-157+155_-157+159del
ENST00000592430.5:n.232+1399_232+1403del
ENST00000593039.5:c.3+1399_3+1403del	ENSP00000466834.1:n.3+1399_3+1403del
NR_037714.1:n.232+1399_232+1403del