Canonical Allele Identifier: CA026149

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394857A>G , CM000675.2:g.32394857A>G	GRCh38
NC_000013.10:g.32968994A>G , CM000675.1:g.32968994A>G	GRCh37
NC_000013.9:g.31866994A>G	NCBI36
NG_012772.3:g.84378A>G , LRG_293:g.84378A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9425A>G MANE Select	NP_000050.3:p.Asp3142Gly
ENST00000380152.8:c.9425A>G MANE Select	ENSP00000369497.3:p.Asp3142Gly
NM_000059.3:c.9425A>G , LRG_293t1:c.9425A>G	NP_000050.2:p.Asp3142Gly
ENST00000380152.7:c.9425A>G	ENSP00000369497.3:p.Asp3142Gly
ENST00000470094.1:c.382A>G
ENST00000470094.2:c.9425A>G	ENSP00000434898.2:p.Asp3142Gly
ENST00000528762.2:c.*792A>G	ENSP00000433168.2:n.*792A>G
ENST00000530893.7:c.9056A>G	ENSP00000499438.2:p.Asp3019Gly
ENST00000544455.5:c.9425A>G	ENSP00000439902.1:p.Asp3142Gly
ENST00000544455.6:c.9425A>G	ENSP00000439902.1:p.Asp3142Gly
ENST00000614259.2:c.9433A>G	ENSP00000506251.1:n.9433A>G
ENST00000665585.1:c.2303A>G
ENST00000665585.2:c.*987A>G	ENSP00000499570.2:n.*987A>G
ENST00000666593.1:c.447A>G	ENSP00000499256.1:n.447A>G
ENST00000666593.2:c.*270A>G	ENSP00000499256.2:n.*270A>G
ENST00000680887.1:c.9425A>G	ENSP00000505508.1:p.Asp3142Gly
ENST00000700202.1:c.1841A>G	ENSP00000514856.1:p.Asp614Gly
ENST00000700202.2:c.9374A>G	ENSP00000514856.2:p.Asp3125Gly
ENST00000700203.1:n.1552A>G
XM_011535203.1:c.9425A>G	XP_011533505.1:p.Asp3142Gly
XM_011535204.1:c.9329A>G	XP_011533506.1:p.Asp3110Gly