Canonical Allele Identifier: CA2082834609

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32378979C= , CM000675.2:g.32378979C=	GRCh38
NC_000013.10:g.32953116C= , CM000675.1:g.32953116C=	GRCh37
NC_000013.9:g.31851116C=	NCBI36
NG_012772.3:g.68500C= , LRG_293:g.68500C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8755-338C=	ENSP00000434898.2:n.8755-338C=
ENST00000528762.2:c.*122-338C=	ENSP00000433168.2:n.*122-338C=
ENST00000530893.7:c.8386-338C=	ENSP00000499438.2:n.8386-338C=
ENST00000665585.2:c.*317-338C=	ENSP00000499570.2:n.*317-338C=
ENST00000666593.2:c.8755-338C=	ENSP00000499256.2:n.8755-338C=
ENST00000700202.2:c.8755-338C=	ENSP00000514856.2:n.8755-338C=
ENST00000700202.1:c.1222-338C=	ENSP00000514856.1:n.1222-338C=
ENST00000700203.1:n.882-338C=
ENST00000380152.8:c.8755-338C= MANE Select	ENSP00000369497.3:n.8755-338C=
ENST00000544455.6:c.8755-338C=	ENSP00000439902.1:n.8755-338C=
ENST00000614259.2:c.8763-338C=	ENSP00000506251.1:n.8763-338C=
ENST00000665585.1:c.1633-338C=
ENST00000680887.1:c.8755-338C=	ENSP00000505508.1:n.8755-338C=
ENST00000380152.7:c.8755-338C=	ENSP00000369497.3:n.8755-338C=
ENST00000528762.1:c.317-338C=	ENSP00000433168.1:n.317-338C=
ENST00000544455.5:c.8755-338C=	ENSP00000439902.1:n.8755-338C=
NM_000059.3:c.8755-338C= , LRG_293t1:c.8755-338C=	NP_000050.2:n.8755-338C=
XM_011535203.1:c.8755-338C=	XP_011533505.1:n.8755-338C=
XM_011535204.1:c.8659-338C=	XP_011533506.1:n.8659-338C=
XM_011535205.1:c.8755-771C=	XP_011533507.1:n.8755-771C=
NM_000059.4:c.8755-338C= MANE Select	NP_000050.3:n.8755-338C=