Canonical Allele Identifier: CA2082831325

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32397150T= , CM000675.2:g.32397150T=	GRCh38
NC_000013.10:g.32971287T= , CM000675.1:g.32971287T=	GRCh37
NC_000013.9:g.31869287T=	NCBI36
NG_012772.3:g.86671T= , LRG_293:g.86671T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*171+106T=	ENSP00000434898.2:n.*171+106T=
ENST00000528762.2:c.*1015+106T=	ENSP00000433168.2:n.*1015+106T=
ENST00000530893.7:c.9279+106T=	ENSP00000499438.2:n.9279+106T=
ENST00000665585.2:c.*1210+106T=	ENSP00000499570.2:n.*1210+106T=
ENST00000700202.2:c.9597+106T=	ENSP00000514856.2:n.9597+106T=
ENST00000700202.1:c.2064+106T=	ENSP00000514856.1:n.2064+106T=
ENST00000700203.1:n.1775+106T=
ENST00000380152.8:c.9648+106T= MANE Select	ENSP00000369497.3:n.9648+106T=
ENST00000544455.6:c.9648+106T=	ENSP00000439902.1:n.9648+106T=
ENST00000614259.2:c.9656+106T=	ENSP00000506251.1:n.9656+106T=
ENST00000665585.1:c.2526+106T=
ENST00000680887.1:c.9648+106T=	ENSP00000505508.1:n.9648+106T=
ENST00000380152.7:c.9648+106T=	ENSP00000369497.3:n.9648+106T=
ENST00000470094.1:c.731+106T=
ENST00000533776.1:n.236+106T=
ENST00000544455.5:c.9648+106T=	ENSP00000439902.1:n.9648+106T=
NM_000059.3:c.9648+106T= , LRG_293t1:c.9648+106T=	NP_000050.2:n.9648+106T=
XM_011535203.1:c.9648+106T=	XP_011533505.1:n.9648+106T=
XM_011535204.1:c.9552+106T=	XP_011533506.1:n.9552+106T=
NM_000059.4:c.9648+106T= MANE Select	NP_000050.3:n.9648+106T=