Canonical Allele Identifier: CA2082835101
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398294G= , CM000675.2:g.32398294G= GRCh38
NC_000013.10:g.32972431G= , CM000675.1:g.32972431G= GRCh37
NC_000013.9:g.31870431G= NCBI36
NG_012772.3:g.87815G= , LRG_293:g.87815G=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*304G= ENSP00000434898.2:n.*304G=
ENST00000528762.2:c.*1148G= ENSP00000433168.2:n.*1148G=
ENST00000530893.7:c.9412G= ENSP00000499438.2:p.Asp3138=
ENST00000665585.2:c.*1343G= ENSP00000499570.2:n.*1343G=
ENST00000700202.2:c.9730G= ENSP00000514856.2:p.Asp3244=
ENST00000700202.1:c.2197G= ENSP00000514856.1:p.Asp733=
ENST00000700203.1:n.1908G=
ENST00000380152.8:c.9781G= MANE Select ENSP00000369497.3:p.Asp3261=
ENST00000544455.6:c.9781G= ENSP00000439902.1:p.Asp3261=
ENST00000614259.2:c.9789G= ENSP00000506251.1:n.9789G=
ENST00000680887.1:c.9781G= ENSP00000505508.1:p.Asp3261=
ENST00000380152.7:c.9781G= ENSP00000369497.3:p.Asp3261=
ENST00000533776.1:n.369G=
ENST00000544455.5:c.9781G= ENSP00000439902.1:p.Asp3261=
NM_000059.3:c.9781G= , LRG_293t1:c.9781G= NP_000050.2:p.Asp3261=
XM_011535203.1:c.9781G= XP_011533505.1:p.Asp3261=
XM_011535204.1:c.9685G= XP_011533506.1:p.Asp3229=
NM_000059.4:c.9781G= MANE Select NP_000050.3:p.Asp3261=