Canonical Allele Identifier: CA387762962

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32396915C>A , CM000675.2:g.32396915C>A	GRCh38
NC_000013.10:g.32971052C>A , CM000675.1:g.32971052C>A	GRCh37
NC_000013.9:g.31869052C>A	NCBI36
NG_012772.3:g.86436C>A , LRG_293:g.86436C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9519C>A MANE Select	NP_000050.3:p.Cys3173Ter
ENST00000380152.8:c.9519C>A MANE Select	ENSP00000369497.3:p.Cys3173Ter
NM_000059.3:c.9519C>A , LRG_293t1:c.9519C>A	NP_000050.2:p.Cys3173Ter
ENST00000380152.7:c.9519C>A	ENSP00000369497.3:p.Cys3173Ter
ENST00000470094.1:c.602C>A
ENST00000470094.2:c.*42C>A	ENSP00000434898.2:n.*42C>A
ENST00000528762.2:c.*886C>A	ENSP00000433168.2:n.*886C>A
ENST00000530893.7:c.9150C>A	ENSP00000499438.2:p.Cys3050Ter
ENST00000533776.1:n.107C>A
ENST00000544455.5:c.9519C>A	ENSP00000439902.1:p.Cys3173Ter
ENST00000544455.6:c.9519C>A	ENSP00000439902.1:p.Cys3173Ter
ENST00000614259.2:c.9527C>A	ENSP00000506251.1:n.9527C>A
ENST00000665585.1:c.2397C>A
ENST00000665585.2:c.*1081C>A	ENSP00000499570.2:n.*1081C>A
ENST00000680887.1:c.9519C>A	ENSP00000505508.1:p.Cys3173Ter
ENST00000700202.1:c.1935C>A	ENSP00000514856.1:p.Cys645Ter
ENST00000700202.2:c.9468C>A	ENSP00000514856.2:p.Cys3156Ter
ENST00000700203.1:n.1646C>A
XM_011535203.1:c.9519C>A	XP_011533505.1:p.Cys3173Ter
XM_011535204.1:c.9423C>A	XP_011533506.1:p.Cys3141Ter