Canonical Allele Identifier: CA025922

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379803G>T , CM000675.2:g.32379803G>T	GRCh38
NC_000013.10:g.32953940G>T , CM000675.1:g.32953940G>T	GRCh37
NC_000013.9:g.31851940G>T	NCBI36
NG_012772.3:g.69324G>T , LRG_293:g.69324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9007G>T	ENSP00000434898.2:p.Gly3003Ter
ENST00000528762.2:c.*374G>T	ENSP00000433168.2:n.*374G>T
ENST00000530893.7:c.8638G>T	ENSP00000499438.2:p.Gly2880Ter
ENST00000665585.2:c.*569G>T	ENSP00000499570.2:n.*569G>T
ENST00000666593.2:c.9007G>T	ENSP00000499256.2:p.Gly3003Ter
ENST00000700202.2:c.8956G>T	ENSP00000514856.2:p.Gly2986Ter
ENST00000700202.1:c.1423G>T	ENSP00000514856.1:p.Gly475Ter
ENST00000700203.1:n.1134G>T
ENST00000380152.8:c.9007G>T MANE Select	ENSP00000369497.3:p.Gly3003Ter
ENST00000544455.6:c.9007G>T	ENSP00000439902.1:p.Gly3003Ter
ENST00000614259.2:c.9015G>T	ENSP00000506251.1:n.9015G>T
ENST00000665585.1:c.1885G>T
ENST00000680887.1:c.9007G>T	ENSP00000505508.1:p.Gly3003Ter
ENST00000380152.7:c.9007G>T	ENSP00000369497.3:p.Gly3003Ter
ENST00000544455.5:c.9007G>T	ENSP00000439902.1:p.Gly3003Ter
NM_000059.3:c.9007G>T , LRG_293t1:c.9007G>T	NP_000050.2:p.Gly3003Ter
XM_011535203.1:c.9007G>T	XP_011533505.1:p.Gly3003Ter
XM_011535204.1:c.8911G>T	XP_011533506.1:p.Gly2971Ter
XM_011535205.1:c.*45G>T	XP_011533507.1:n.*45G>T
NM_000059.4:c.9007G>T MANE Select	NP_000050.3:p.Gly3003Ter