Canonical Allele Identifier: CA387761842

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394919A>T , CM000675.2:g.32394919A>T	GRCh38
NC_000013.10:g.32969056A>T , CM000675.1:g.32969056A>T	GRCh37
NC_000013.9:g.31867056A>T	NCBI36
NG_012772.3:g.84440A>T , LRG_293:g.84440A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9487A>T MANE Select	NP_000050.3:p.Lys3163Ter
ENST00000380152.8:c.9487A>T MANE Select	ENSP00000369497.3:p.Lys3163Ter
NM_000059.3:c.9487A>T , LRG_293t1:c.9487A>T	NP_000050.2:p.Lys3163Ter
ENST00000380152.7:c.9487A>T	ENSP00000369497.3:p.Lys3163Ter
ENST00000470094.1:c.444A>T
ENST00000470094.2:c.9487A>T	ENSP00000434898.2:p.Lys3163Ter
ENST00000528762.2:c.*854A>T	ENSP00000433168.2:n.*854A>T
ENST00000530893.7:c.9118A>T	ENSP00000499438.2:p.Lys3040Ter
ENST00000544455.5:c.9487A>T	ENSP00000439902.1:p.Lys3163Ter
ENST00000544455.6:c.9487A>T	ENSP00000439902.1:p.Lys3163Ter
ENST00000614259.2:c.9495A>T	ENSP00000506251.1:n.9495A>T
ENST00000665585.1:c.2365A>T
ENST00000665585.2:c.*1049A>T	ENSP00000499570.2:n.*1049A>T
ENST00000666593.1:c.509A>T	ENSP00000499256.1:n.509A>T
ENST00000666593.2:c.*332A>T	ENSP00000499256.2:n.*332A>T
ENST00000680887.1:c.9487A>T	ENSP00000505508.1:p.Lys3163Ter
ENST00000700202.1:c.1903A>T	ENSP00000514856.1:p.Lys635Ter
ENST00000700202.2:c.9436A>T	ENSP00000514856.2:p.Lys3146Ter
ENST00000700203.1:n.1614A>T
XM_011535203.1:c.9487A>T	XP_011533505.1:p.Lys3163Ter
XM_011535204.1:c.9391A>T	XP_011533506.1:p.Lys3131Ter