Canonical Allele Identifier: CA2082839580

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32399176C= , CM000675.2:g.32399176C=	GRCh38
NC_000013.10:g.32973313C= , CM000675.1:g.32973313C=	GRCh37
NC_000013.9:g.31871313C=	NCBI36
NG_012772.3:g.88697C= , LRG_293:g.88697C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*1186C=	ENSP00000434898.2:n.*1186C=
ENST00000530893.7:c.*406C=	ENSP00000499438.2:n.*406C=
ENST00000380152.8:c.*406C= MANE Select	ENSP00000369497.3:n.*406C=
ENST00000544455.6:c.*406C=	ENSP00000439902.1:n.*406C=
ENST00000614259.2:c.10671C=	ENSP00000506251.1:n.10671C=
ENST00000680887.1:c.*406C=	ENSP00000505508.1:n.*406C=
ENST00000380152.7:c.*406C=	ENSP00000369497.3:n.*406C=
ENST00000544455.5:c.*406C=	ENSP00000439902.1:n.*406C=
NM_000059.3:c.*406C= , LRG_293t1:c.*406C=	NP_000050.2:n.*406C=
XM_011535203.1:c.*406C=	XP_011533505.1:n.*406C=
XM_011535204.1:c.*406C=	XP_011533506.1:n.*406C=
NM_000059.4:c.*406C= MANE Select	NP_000050.3:n.*406C=