Canonical Allele Identifier: CA2082835935

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398426G= , CM000675.2:g.32398426G=	GRCh38
NC_000013.10:g.32972563G= , CM000675.1:g.32972563G=	GRCh37
NC_000013.9:g.31870563G=	NCBI36
NG_012772.3:g.87947G= , LRG_293:g.87947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*436G=	ENSP00000434898.2:n.*436G=
ENST00000528762.2:c.*1280G=	ENSP00000433168.2:n.*1280G=
ENST00000530893.7:c.9544G=	ENSP00000499438.2:p.Gly3182=
ENST00000665585.2:c.*1475G=	ENSP00000499570.2:n.*1475G=
ENST00000700202.2:c.9862G=	ENSP00000514856.2:p.Gly3288=
ENST00000700202.1:c.2329G=	ENSP00000514856.1:p.Gly777=
ENST00000700203.1:n.2040G=
ENST00000380152.8:c.9913G= MANE Select	ENSP00000369497.3:p.Gly3305=
ENST00000544455.6:c.9913G=	ENSP00000439902.1:p.Gly3305=
ENST00000614259.2:c.9921G=	ENSP00000506251.1:n.9921G=
ENST00000680887.1:c.9913G=	ENSP00000505508.1:p.Gly3305=
ENST00000380152.7:c.9913G=	ENSP00000369497.3:p.Gly3305=
ENST00000533776.1:n.501G=
ENST00000544455.5:c.9913G=	ENSP00000439902.1:p.Gly3305=
NM_000059.3:c.9913G= , LRG_293t1:c.9913G=	NP_000050.2:p.Gly3305=
XM_011535203.1:c.9913G=	XP_011533505.1:p.Gly3305=
XM_011535204.1:c.9817G=	XP_011533506.1:p.Gly3273=
NM_000059.4:c.9913G= MANE Select	NP_000050.3:p.Gly3305=