Canonical Allele Identifier: CA2082836142

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398457A= , CM000675.2:g.32398457A=	GRCh38
NC_000013.10:g.32972594A= , CM000675.1:g.32972594A=	GRCh37
NC_000013.9:g.31870594A=	NCBI36
NG_012772.3:g.87978A= , LRG_293:g.87978A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*467A=	ENSP00000434898.2:n.*467A=
ENST00000528762.2:c.*1311A=	ENSP00000433168.2:n.*1311A=
ENST00000530893.7:c.9575A=	ENSP00000499438.2:p.Lys3192=
ENST00000665585.2:c.*1506A=	ENSP00000499570.2:n.*1506A=
ENST00000700202.2:c.9893A=	ENSP00000514856.2:p.Lys3298=
ENST00000700202.1:c.2360A=	ENSP00000514856.1:p.Lys787=
ENST00000700203.1:n.2071A=
ENST00000380152.8:c.9944A= MANE Select	ENSP00000369497.3:p.Lys3315=
ENST00000544455.6:c.9944A=	ENSP00000439902.1:p.Lys3315=
ENST00000614259.2:c.9952A=	ENSP00000506251.1:n.9952A=
ENST00000680887.1:c.9944A=	ENSP00000505508.1:p.Lys3315=
ENST00000380152.7:c.9944A=	ENSP00000369497.3:p.Lys3315=
ENST00000544455.5:c.9944A=	ENSP00000439902.1:p.Lys3315=
NM_000059.3:c.9944A= , LRG_293t1:c.9944A=	NP_000050.2:p.Lys3315=
XM_011535203.1:c.9944A=	XP_011533505.1:p.Lys3315=
XM_011535204.1:c.9848A=	XP_011533506.1:p.Lys3283=
NM_000059.4:c.9944A= MANE Select	NP_000050.3:p.Lys3315=