Canonical Allele Identifier: CA2082836666

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398549T= , CM000675.2:g.32398549T=	GRCh38
NC_000013.10:g.32972686T= , CM000675.1:g.32972686T=	GRCh37
NC_000013.9:g.31870686T=	NCBI36
NG_012772.3:g.88070T= , LRG_293:g.88070T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*559T=	ENSP00000434898.2:n.*559T=
ENST00000528762.2:c.*1403T=	ENSP00000433168.2:n.*1403T=
ENST00000530893.7:c.9667T=	ENSP00000499438.2:p.Leu3223=
ENST00000665585.2:c.*1598T=	ENSP00000499570.2:n.*1598T=
ENST00000700202.2:c.9985T=	ENSP00000514856.2:p.Leu3329=
ENST00000700202.1:c.2452T=	ENSP00000514856.1:p.Leu818=
ENST00000700203.1:n.2163T=
ENST00000380152.8:c.10036T= MANE Select	ENSP00000369497.3:p.Leu3346=
ENST00000544455.6:c.10036T=	ENSP00000439902.1:p.Leu3346=
ENST00000614259.2:c.10044T=	ENSP00000506251.1:n.10044T=
ENST00000680887.1:c.10036T=	ENSP00000505508.1:p.Leu3346=
ENST00000380152.7:c.10036T=	ENSP00000369497.3:p.Leu3346=
ENST00000544455.5:c.10036T=	ENSP00000439902.1:p.Leu3346=
NM_000059.3:c.10036T= , LRG_293t1:c.10036T=	NP_000050.2:p.Leu3346=
XM_011535203.1:c.10036T=	XP_011533505.1:p.Leu3346=
XM_011535204.1:c.9940T=	XP_011533506.1:p.Leu3314=
NM_000059.4:c.10036T= MANE Select	NP_000050.3:p.Leu3346=