Canonical Allele Identifier: CA022572

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 51879
• ClinVar RCV Id: RCV000044681 ; RCV000241060 ; RCV000580714
• dbSNP Id: rs397507787
• MyVariant Identifiers: chr13:g.32914052_32914053del (hg19) ; chr13:g.32339915_32339916del (hg38)
• PubMed: PMID:17262179

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339915_32339916del , CM000675.2:g.32339915_32339916del	GRCh38
NC_000013.10:g.32914052_32914053del , CM000675.1:g.32914052_32914053del	GRCh37
NC_000013.9:g.31812052_31812053del	NCBI36
NG_012772.3:g.29436_29437del , LRG_293:g.29436_29437del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.5560_5561del	ENSP00000434898.2:p.Val1854PhefsTer3
ENST00000528762.2:c.5560_5561del	ENSP00000433168.2:p.Val1854PhefsTer3
ENST00000530893.7:c.5191_5192del	ENSP00000499438.2:p.Val1731PhefsTer3
ENST00000665585.2:c.5560_5561del	ENSP00000499570.2:p.Val1854PhefsTer3
ENST00000666593.2:c.5560_5561del	ENSP00000499256.2:p.Val1854PhefsTer3
ENST00000700202.2:c.5560_5561del	ENSP00000514856.2:p.Val1854PhefsTer3
ENST00000380152.8:c.5560_5561del MANE Select	ENSP00000369497.3:p.Val1854PhefsTer3
ENST00000544455.6:c.5560_5561del	ENSP00000439902.1:p.Val1854PhefsTer3
ENST00000614259.2:c.5560_5561del	ENSP00000506251.1:p.Val1854PhefsTer3
ENST00000680887.1:c.5560_5561del	ENSP00000505508.1:p.Val1854PhefsTer3
ENST00000380152.7:c.5560_5561del	ENSP00000369497.3:p.Val1854PhefsTer3
ENST00000544455.5:c.5560_5561del	ENSP00000439902.1:p.Val1854PhefsTer3
ENST00000614259.1:n.5560_5561del
NM_000059.3:c.5560_5561del , LRG_293t1:c.5560_5561del	NP_000050.2:p.Val1854PhefsTer3
XM_011535203.1:c.5560_5561del	XP_011533505.1:p.Val1854PhefsTer3
XM_011535204.1:c.5560_5561del	XP_011533506.1:p.Val1854PhefsTer3
XM_011535205.1:c.5560_5561del	XP_011533507.1:p.Val1854PhefsTer3
NM_000059.4:c.5560_5561del MANE Select	NP_000050.3:p.Val1854PhefsTer3