Canonical Allele Identifier: CA2082838715

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379866A= , CM000675.2:g.32379866A=	GRCh38
NC_000013.10:g.32954003A= , CM000675.1:g.32954003A=	GRCh37
NC_000013.9:g.31852003A=	NCBI36
NG_012772.3:g.69387A= , LRG_293:g.69387A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9070A=	ENSP00000434898.2:p.Asn3024=
ENST00000528762.2:c.*437A=	ENSP00000433168.2:n.*437A=
ENST00000530893.7:c.8701A=	ENSP00000499438.2:p.Asn2901=
ENST00000665585.2:c.*632A=	ENSP00000499570.2:n.*632A=
ENST00000666593.2:c.9070A=	ENSP00000499256.2:p.Asn3024=
ENST00000700202.2:c.9019A=	ENSP00000514856.2:p.Asn3007=
ENST00000700202.1:c.1486A=	ENSP00000514856.1:p.Asn496=
ENST00000700203.1:n.1197A=
ENST00000380152.8:c.9070A= MANE Select	ENSP00000369497.3:p.Asn3024=
ENST00000544455.6:c.9070A=	ENSP00000439902.1:p.Asn3024=
ENST00000614259.2:c.9078A=	ENSP00000506251.1:n.9078A=
ENST00000665585.1:c.1948A=
ENST00000680887.1:c.9070A=	ENSP00000505508.1:p.Asn3024=
ENST00000380152.7:c.9070A=	ENSP00000369497.3:p.Asn3024=
ENST00000470094.1:c.27A=
ENST00000544455.5:c.9070A=	ENSP00000439902.1:p.Asn3024=
NM_000059.3:c.9070A= , LRG_293t1:c.9070A=	NP_000050.2:p.Asn3024=
XM_011535203.1:c.9070A=	XP_011533505.1:p.Asn3024=
XM_011535204.1:c.8974A=	XP_011533506.1:p.Asn2992=
NM_000059.4:c.9070A= MANE Select	NP_000050.3:p.Asn3024=