Canonical Allele Identifier: CA2082835440

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398349T= , CM000675.2:g.32398349T=	GRCh38
NC_000013.10:g.32972486T= , CM000675.1:g.32972486T=	GRCh37
NC_000013.9:g.31870486T=	NCBI36
NG_012772.3:g.87870T= , LRG_293:g.87870T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*359T=	ENSP00000434898.2:n.*359T=
ENST00000528762.2:c.*1203T=	ENSP00000433168.2:n.*1203T=
ENST00000530893.7:c.9467T=	ENSP00000499438.2:p.Leu3156=
ENST00000665585.2:c.*1398T=	ENSP00000499570.2:n.*1398T=
ENST00000700202.2:c.9785T=	ENSP00000514856.2:p.Leu3262=
ENST00000700202.1:c.2252T=	ENSP00000514856.1:p.Leu751=
ENST00000700203.1:n.1963T=
ENST00000380152.8:c.9836T= MANE Select	ENSP00000369497.3:p.Leu3279=
ENST00000544455.6:c.9836T=	ENSP00000439902.1:p.Leu3279=
ENST00000614259.2:c.9844T=	ENSP00000506251.1:n.9844T=
ENST00000680887.1:c.9836T=	ENSP00000505508.1:p.Leu3279=
ENST00000380152.7:c.9836T=	ENSP00000369497.3:p.Leu3279=
ENST00000533776.1:n.424T=
ENST00000544455.5:c.9836T=	ENSP00000439902.1:p.Leu3279=
NM_000059.3:c.9836T= , LRG_293t1:c.9836T=	NP_000050.2:p.Leu3279=
XM_011535203.1:c.9836T=	XP_011533505.1:p.Leu3279=
XM_011535204.1:c.9740T=	XP_011533506.1:p.Leu3247=
NM_000059.4:c.9836T= MANE Select	NP_000050.3:p.Leu3279=