Canonical Allele Identifier: CA2082835499

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398355C= , CM000675.2:g.32398355C=	GRCh38
NC_000013.10:g.32972492C= , CM000675.1:g.32972492C=	GRCh37
NC_000013.9:g.31870492C=	NCBI36
NG_012772.3:g.87876C= , LRG_293:g.87876C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*365C=	ENSP00000434898.2:n.*365C=
ENST00000528762.2:c.*1209C=	ENSP00000433168.2:n.*1209C=
ENST00000530893.7:c.9473C=	ENSP00000499438.2:p.Pro3158=
ENST00000665585.2:c.*1404C=	ENSP00000499570.2:n.*1404C=
ENST00000700202.2:c.9791C=	ENSP00000514856.2:p.Pro3264=
ENST00000700202.1:c.2258C=	ENSP00000514856.1:p.Pro753=
ENST00000700203.1:n.1969C=
ENST00000380152.8:c.9842C= MANE Select	ENSP00000369497.3:p.Pro3281=
ENST00000544455.6:c.9842C=	ENSP00000439902.1:p.Pro3281=
ENST00000614259.2:c.9850C=	ENSP00000506251.1:n.9850C=
ENST00000680887.1:c.9842C=	ENSP00000505508.1:p.Pro3281=
ENST00000380152.7:c.9842C=	ENSP00000369497.3:p.Pro3281=
ENST00000533776.1:n.430C=
ENST00000544455.5:c.9842C=	ENSP00000439902.1:p.Pro3281=
NM_000059.3:c.9842C= , LRG_293t1:c.9842C=	NP_000050.2:p.Pro3281=
XM_011535203.1:c.9842C=	XP_011533505.1:p.Pro3281=
XM_011535204.1:c.9746C=	XP_011533506.1:p.Pro3249=
NM_000059.4:c.9842C= MANE Select	NP_000050.3:p.Pro3281=