Canonical Allele Identifier: CA6941469

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398583C>G , CM000675.2:g.32398583C>G	GRCh38
NC_000013.10:g.32972720C>G , CM000675.1:g.32972720C>G	GRCh37
NC_000013.9:g.31870720C>G	NCBI36
NG_012772.3:g.88104C>G , LRG_293:g.88104C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.10070C>G MANE Select	NP_000050.3:p.Thr3357Arg
ENST00000380152.8:c.10070C>G MANE Select	ENSP00000369497.3:p.Thr3357Arg
NM_000059.3:c.10070C>G , LRG_293t1:c.10070C>G	NP_000050.2:p.Thr3357Arg
ENST00000380152.7:c.10070C>G	ENSP00000369497.3:p.Thr3357Arg
ENST00000470094.2:c.*593C>G	ENSP00000434898.2:n.*593C>G
ENST00000528762.2:c.*1437C>G	ENSP00000433168.2:n.*1437C>G
ENST00000530893.7:c.9701C>G	ENSP00000499438.2:p.Thr3234Arg
ENST00000544455.5:c.10070C>G	ENSP00000439902.1:p.Thr3357Arg
ENST00000544455.6:c.10070C>G	ENSP00000439902.1:p.Thr3357Arg
ENST00000614259.2:c.10078C>G	ENSP00000506251.1:n.10078C>G
ENST00000665585.2:c.*1632C>G	ENSP00000499570.2:n.*1632C>G
ENST00000680887.1:c.10070C>G	ENSP00000505508.1:p.Thr3357Arg
ENST00000700202.1:c.2486C>G	ENSP00000514856.1:p.Thr829Arg
ENST00000700202.2:c.10019C>G	ENSP00000514856.2:p.Thr3340Arg
ENST00000700203.1:n.2197C>G
XM_011535203.1:c.10070C>G	XP_011533505.1:p.Thr3357Arg
XM_011535204.1:c.9974C>G	XP_011533506.1:p.Thr3325Arg