Canonical Allele Identifier: CA2082835711

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379374G= , CM000675.2:g.32379374G=	GRCh38
NC_000013.10:g.32953511G= , CM000675.1:g.32953511G=	GRCh37
NC_000013.9:g.31851511G=	NCBI36
NG_012772.3:g.68895G= , LRG_293:g.68895G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8812G=	ENSP00000434898.2:p.Asp2938=
ENST00000528762.2:c.*179G=	ENSP00000433168.2:n.*179G=
ENST00000530893.7:c.8443G=	ENSP00000499438.2:p.Asp2815=
ENST00000665585.2:c.*374G=	ENSP00000499570.2:n.*374G=
ENST00000666593.2:c.8812G=	ENSP00000499256.2:p.Asp2938=
ENST00000700202.2:c.8812G=	ENSP00000514856.2:p.Asp2938=
ENST00000700202.1:c.1279G=	ENSP00000514856.1:p.Asp427=
ENST00000700203.1:n.939G=
ENST00000380152.8:c.8812G= MANE Select	ENSP00000369497.3:p.Asp2938=
ENST00000544455.6:c.8812G=	ENSP00000439902.1:p.Asp2938=
ENST00000614259.2:c.8820G=	ENSP00000506251.1:n.8820G=
ENST00000665585.1:c.1690G=
ENST00000680887.1:c.8812G=	ENSP00000505508.1:p.Asp2938=
ENST00000380152.7:c.8812G=	ENSP00000369497.3:p.Asp2938=
ENST00000528762.1:c.374G=	ENSP00000433168.1:n.374G=
ENST00000544455.5:c.8812G=	ENSP00000439902.1:p.Asp2938=
NM_000059.3:c.8812G= , LRG_293t1:c.8812G=	NP_000050.2:p.Asp2938=
XM_011535203.1:c.8812G=	XP_011533505.1:p.Asp2938=
XM_011535204.1:c.8716G=	XP_011533506.1:p.Asp2906=
XM_011535205.1:c.8755-376G=	XP_011533507.1:n.8755-376G=
NM_000059.4:c.8812G= MANE Select	NP_000050.3:p.Asp2938=