Canonical Allele Identifier: CA2082837637

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379770C= , CM000675.2:g.32379770C=	GRCh38
NC_000013.10:g.32953907C= , CM000675.1:g.32953907C=	GRCh37
NC_000013.9:g.31851907C=	NCBI36
NG_012772.3:g.69291C= , LRG_293:g.69291C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8974C=	ENSP00000434898.2:p.Pro2992=
ENST00000528762.2:c.*341C=	ENSP00000433168.2:n.*341C=
ENST00000530893.7:c.8605C=	ENSP00000499438.2:p.Pro2869=
ENST00000665585.2:c.*536C=	ENSP00000499570.2:n.*536C=
ENST00000666593.2:c.8974C=	ENSP00000499256.2:p.Pro2992=
ENST00000700202.2:c.8954-31C=	ENSP00000514856.2:n.8954-31C=
ENST00000700202.1:c.1421-31C=	ENSP00000514856.1:n.1421-31C=
ENST00000700203.1:n.1101C=
ENST00000380152.8:c.8974C= MANE Select	ENSP00000369497.3:p.Pro2992=
ENST00000544455.6:c.8974C=	ENSP00000439902.1:p.Pro2992=
ENST00000614259.2:c.8982C=	ENSP00000506251.1:n.8982C=
ENST00000665585.1:c.1852C=
ENST00000680887.1:c.8974C=	ENSP00000505508.1:p.Pro2992=
ENST00000380152.7:c.8974C=	ENSP00000369497.3:p.Pro2992=
ENST00000544455.5:c.8974C=	ENSP00000439902.1:p.Pro2992=
NM_000059.3:c.8974C= , LRG_293t1:c.8974C=	NP_000050.2:p.Pro2992=
XM_011535203.1:c.8974C=	XP_011533505.1:p.Pro2992=
XM_011535204.1:c.8878C=	XP_011533506.1:p.Pro2960=
XM_011535205.1:c.*12C=	XP_011533507.1:n.*12C=
NM_000059.4:c.8974C= MANE Select	NP_000050.3:p.Pro2992=