Canonical Allele Identifier: CA2082835688

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398387C= , CM000675.2:g.32398387C=	GRCh38
NC_000013.10:g.32972524C= , CM000675.1:g.32972524C=	GRCh37
NC_000013.9:g.31870524C=	NCBI36
NG_012772.3:g.87908C= , LRG_293:g.87908C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*397C=	ENSP00000434898.2:n.*397C=
ENST00000528762.2:c.*1241C=	ENSP00000433168.2:n.*1241C=
ENST00000530893.7:c.9505C=	ENSP00000499438.2:p.Pro3169=
ENST00000665585.2:c.*1436C=	ENSP00000499570.2:n.*1436C=
ENST00000700202.2:c.9823C=	ENSP00000514856.2:p.Pro3275=
ENST00000700202.1:c.2290C=	ENSP00000514856.1:p.Pro764=
ENST00000700203.1:n.2001C=
ENST00000380152.8:c.9874C= MANE Select	ENSP00000369497.3:p.Pro3292=
ENST00000544455.6:c.9874C=	ENSP00000439902.1:p.Pro3292=
ENST00000614259.2:c.9882C=	ENSP00000506251.1:n.9882C=
ENST00000680887.1:c.9874C=	ENSP00000505508.1:p.Pro3292=
ENST00000380152.7:c.9874C=	ENSP00000369497.3:p.Pro3292=
ENST00000533776.1:n.462C=
ENST00000544455.5:c.9874C=	ENSP00000439902.1:p.Pro3292=
NM_000059.3:c.9874C= , LRG_293t1:c.9874C=	NP_000050.2:p.Pro3292=
XM_011535203.1:c.9874C=	XP_011533505.1:p.Pro3292=
XM_011535204.1:c.9778C=	XP_011533506.1:p.Pro3260=
NM_000059.4:c.9874C= MANE Select	NP_000050.3:p.Pro3292=