Canonical Allele Identifier: CA026000

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32380014A>G , CM000675.2:g.32380014A>G	GRCh38
NC_000013.10:g.32954151A>G , CM000675.1:g.32954151A>G	GRCh37
NC_000013.9:g.31852151A>G	NCBI36
NG_012772.3:g.69535A>G , LRG_293:g.69535A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9125A>G MANE Select	NP_000050.3:p.Asp3042Gly
ENST00000380152.8:c.9125A>G MANE Select	ENSP00000369497.3:p.Asp3042Gly
NM_000059.3:c.9125A>G , LRG_293t1:c.9125A>G	NP_000050.2:p.Asp3042Gly
ENST00000380152.7:c.9125A>G	ENSP00000369497.3:p.Asp3042Gly
ENST00000470094.1:c.82A>G
ENST00000470094.2:c.9125A>G	ENSP00000434898.2:p.Asp3042Gly
ENST00000528762.2:c.*492A>G	ENSP00000433168.2:n.*492A>G
ENST00000530893.7:c.8756A>G	ENSP00000499438.2:p.Asp2919Gly
ENST00000544455.5:c.9125A>G	ENSP00000439902.1:p.Asp3042Gly
ENST00000544455.6:c.9125A>G	ENSP00000439902.1:p.Asp3042Gly
ENST00000614259.2:c.9133A>G	ENSP00000506251.1:n.9133A>G
ENST00000665585.1:c.2003A>G
ENST00000665585.2:c.*687A>G	ENSP00000499570.2:n.*687A>G
ENST00000666593.1:c.8A>G	ENSP00000499256.1:p.Asp3Gly
ENST00000666593.2:c.9125A>G	ENSP00000499256.2:p.Asp3042Gly
ENST00000680887.1:c.9125A>G	ENSP00000505508.1:p.Asp3042Gly
ENST00000700202.1:c.1541A>G	ENSP00000514856.1:p.Asp514Gly
ENST00000700202.2:c.9074A>G	ENSP00000514856.2:p.Asp3025Gly
ENST00000700203.1:n.1252A>G
XM_011535203.1:c.9125A>G	XP_011533505.1:p.Asp3042Gly
XM_011535204.1:c.9029A>G	XP_011533506.1:p.Asp3010Gly