Canonical Allele Identifier: CA2082822213
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394718G= , CM000675.2:g.32394718G= GRCh38
NC_000013.10:g.32968855G= , CM000675.1:g.32968855G= GRCh37
NC_000013.9:g.31866855G= NCBI36
NG_012772.3:g.84239G= , LRG_293:g.84239G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.9286G= ENSP00000434898.2:p.Glu3096=
ENST00000528762.2:c.*653G= ENSP00000433168.2:n.*653G=
ENST00000530893.7:c.8917G= ENSP00000499438.2:p.Glu2973=
ENST00000665585.2:c.*848G= ENSP00000499570.2:n.*848G=
ENST00000666593.2:c.*131G= ENSP00000499256.2:n.*131G=
ENST00000700202.2:c.9235G= ENSP00000514856.2:p.Glu3079=
ENST00000700202.1:c.1702G= ENSP00000514856.1:p.Glu568=
ENST00000700203.1:n.1413G=
ENST00000380152.8:c.9286G= MANE Select ENSP00000369497.3:p.Glu3096=
ENST00000544455.6:c.9286G= ENSP00000439902.1:p.Glu3096=
ENST00000614259.2:c.9294G= ENSP00000506251.1:n.9294G=
ENST00000665585.1:c.2164G=
ENST00000666593.1:c.308G= ENSP00000499256.1:n.308G=
ENST00000680887.1:c.9286G= ENSP00000505508.1:p.Glu3096=
ENST00000380152.7:c.9286G= ENSP00000369497.3:p.Glu3096=
ENST00000470094.1:c.243G=
ENST00000544455.5:c.9286G= ENSP00000439902.1:p.Glu3096=
NM_000059.3:c.9286G= , LRG_293t1:c.9286G= NP_000050.2:p.Glu3096=
XM_011535203.1:c.9286G= XP_011533505.1:p.Glu3096=
XM_011535204.1:c.9190G= XP_011533506.1:p.Glu3064=
NM_000059.4:c.9286G= MANE Select NP_000050.3:p.Glu3096=