Canonical Allele Identifier: CA025745

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 91730
• ClinVar RCV Id: RCV000077638 ; RCV000131955 ; RCV000240702 ; RCV001340616 ; RCV001255558 ; RCV002250555
• dbSNP Id: rs398122710
• MyVariant Identifiers: chr13:g.32945237G>A (hg19) ; chr13:g.32371100G>A (hg38)
• PubMed: PMID:27257965

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371100G>A , CM000675.2:g.32371100G>A	GRCh38
NC_000013.10:g.32945237G>A , CM000675.1:g.32945237G>A	GRCh37
NC_000013.9:g.31843237G>A	NCBI36
NG_012772.3:g.60621G>A , LRG_293:g.60621G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8632G>A	ENSP00000434898.2:p.Glu2878Lys
ENST00000528762.2:c.8632G>A	ENSP00000433168.2:p.Val2878Ile
ENST00000530893.7:c.8263G>A	ENSP00000499438.2:p.Glu2755Lys
ENST00000665585.2:c.8632G>A	ENSP00000499570.2:p.Val2878Ile
ENST00000666593.2:c.8632G>A	ENSP00000499256.2:p.Glu2878Lys
ENST00000700202.2:c.8632G>A	ENSP00000514856.2:p.Glu2878Lys
ENST00000700202.1:c.1099G>A	ENSP00000514856.1:p.Glu367Lys
ENST00000380152.8:c.8632G>A MANE Select	ENSP00000369497.3:p.Glu2878Lys
ENST00000544455.6:c.8632G>A	ENSP00000439902.1:p.Glu2878Lys
ENST00000614259.2:c.8640G>A	ENSP00000506251.1:n.8640G>A
ENST00000665585.1:c.1197G>A
ENST00000680887.1:c.8632G>A	ENSP00000505508.1:p.Glu2878Lys
ENST00000380152.7:c.8632G>A	ENSP00000369497.3:p.Glu2878Lys
ENST00000528762.1:c.130G>A	ENSP00000433168.1:p.Val44Ile
ENST00000544455.5:c.8632G>A	ENSP00000439902.1:p.Glu2878Lys
NM_000059.3:c.8632G>A , LRG_293t1:c.8632G>A	NP_000050.2:p.Glu2878Lys
XM_011535203.1:c.8632G>A	XP_011533505.1:p.Glu2878Lys
XM_011535204.1:c.8536G>A	XP_011533506.1:p.Glu2846Lys
XM_011535205.1:c.8632G>A	XP_011533507.1:p.Glu2878Lys
NM_000059.4:c.8632G>A MANE Select	NP_000050.3:p.Glu2878Lys