Canonical Allele Identifier: CA2082836434

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379480G= , CM000675.2:g.32379480G=	GRCh38
NC_000013.10:g.32953617G= , CM000675.1:g.32953617G=	GRCh37
NC_000013.9:g.31851617G=	NCBI36
NG_012772.3:g.69001G= , LRG_293:g.69001G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8918G=	ENSP00000434898.2:p.Arg2973=
ENST00000528762.2:c.*285G=	ENSP00000433168.2:n.*285G=
ENST00000530893.7:c.8549G=	ENSP00000499438.2:p.Arg2850=
ENST00000665585.2:c.*480G=	ENSP00000499570.2:n.*480G=
ENST00000666593.2:c.8918G=	ENSP00000499256.2:p.Arg2973=
ENST00000700202.2:c.8918G=	ENSP00000514856.2:p.Arg2973=
ENST00000700202.1:c.1385G=	ENSP00000514856.1:p.Arg462=
ENST00000700203.1:n.1045G=
ENST00000380152.8:c.8918G= MANE Select	ENSP00000369497.3:p.Arg2973=
ENST00000544455.6:c.8918G=	ENSP00000439902.1:p.Arg2973=
ENST00000614259.2:c.8926G=	ENSP00000506251.1:n.8926G=
ENST00000665585.1:c.1796G=
ENST00000680887.1:c.8918G=	ENSP00000505508.1:p.Arg2973=
ENST00000380152.7:c.8918G=	ENSP00000369497.3:p.Arg2973=
ENST00000528762.1:c.480G=	ENSP00000433168.1:n.480G=
ENST00000544455.5:c.8918G=	ENSP00000439902.1:p.Arg2973=
NM_000059.3:c.8918G= , LRG_293t1:c.8918G=	NP_000050.2:p.Arg2973=
XM_011535203.1:c.8918G=	XP_011533505.1:p.Arg2973=
XM_011535204.1:c.8822G=	XP_011533506.1:p.Arg2941=
XM_011535205.1:c.8755-270G=	XP_011533507.1:n.8755-270G=
NM_000059.4:c.8918G= MANE Select	NP_000050.3:p.Arg2973=