Canonical Allele Identifier: CA2082809296

Gene: BRCA2

Linked Data

• dbSNP Id: rs2072459552

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32336886_32336887insCC , CM000675.2:g.32336886_32336887insCC	GRCh38
NC_000013.10:g.32911023_32911024insCC , CM000675.1:g.32911023_32911024insCC	GRCh37
NC_000013.9:g.31809023_31809024insCC	NCBI36
NG_012772.3:g.26407_26408insCC , LRG_293:g.26407_26408insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2531_2532insCC	ENSP00000434898.2:p.Pro845HisfsTer14
ENST00000528762.2:c.2531_2532insCC	ENSP00000433168.2:p.Pro845HisfsTer14
ENST00000530893.7:c.2162_2163insCC	ENSP00000499438.2:p.Pro722HisfsTer14
ENST00000665585.2:c.2531_2532insCC	ENSP00000499570.2:p.Pro845HisfsTer14
ENST00000666593.2:c.2531_2532insCC	ENSP00000499256.2:p.Pro845HisfsTer14
ENST00000700202.2:c.2531_2532insCC	ENSP00000514856.2:p.Pro845HisfsTer14
ENST00000380152.8:c.2531_2532insCC MANE Select	ENSP00000369497.3:p.Pro845HisfsTer14
ENST00000544455.6:c.2531_2532insCC	ENSP00000439902.1:p.Pro845HisfsTer14
ENST00000614259.2:c.2531_2532insCC	ENSP00000506251.1:p.Pro845HisfsTer14
ENST00000680887.1:c.2531_2532insCC	ENSP00000505508.1:p.Pro845HisfsTer14
ENST00000380152.7:c.2531_2532insCC	ENSP00000369497.3:p.Pro845HisfsTer14
ENST00000544455.5:c.2531_2532insCC	ENSP00000439902.1:p.Pro845HisfsTer14
ENST00000614259.1:n.2531_2532insCC
NM_000059.3:c.2531_2532insCC , LRG_293t1:c.2531_2532insCC	NP_000050.2:p.Pro845HisfsTer14
XM_011535203.1:c.2531_2532insCC	XP_011533505.1:p.Pro845HisfsTer14
XM_011535204.1:c.2531_2532insCC	XP_011533506.1:p.Pro845HisfsTer14
XM_011535205.1:c.2531_2532insCC	XP_011533507.1:p.Pro845HisfsTer14
NM_000059.4:c.2531_2532insCC MANE Select	NP_000050.3:p.Pro845HisfsTer14