Canonical Allele Identifier: CA2082835152
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398299A= , CM000675.2:g.32398299A= GRCh38
NC_000013.10:g.32972436A= , CM000675.1:g.32972436A= GRCh37
NC_000013.9:g.31870436A= NCBI36
NG_012772.3:g.87820A= , LRG_293:g.87820A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*309A= ENSP00000434898.2:n.*309A=
ENST00000528762.2:c.*1153A= ENSP00000433168.2:n.*1153A=
ENST00000530893.7:c.9417A= ENSP00000499438.2:p.Gln3139=
ENST00000665585.2:c.*1348A= ENSP00000499570.2:n.*1348A=
ENST00000700202.2:c.9735A= ENSP00000514856.2:p.Gln3245=
ENST00000700202.1:c.2202A= ENSP00000514856.1:p.Gln734=
ENST00000700203.1:n.1913A=
ENST00000380152.8:c.9786A= MANE Select ENSP00000369497.3:p.Gln3262=
ENST00000544455.6:c.9786A= ENSP00000439902.1:p.Gln3262=
ENST00000614259.2:c.9794A= ENSP00000506251.1:n.9794A=
ENST00000680887.1:c.9786A= ENSP00000505508.1:p.Gln3262=
ENST00000380152.7:c.9786A= ENSP00000369497.3:p.Gln3262=
ENST00000533776.1:n.374A=
ENST00000544455.5:c.9786A= ENSP00000439902.1:p.Gln3262=
NM_000059.3:c.9786A= , LRG_293t1:c.9786A= NP_000050.2:p.Gln3262=
XM_011535203.1:c.9786A= XP_011533505.1:p.Gln3262=
XM_011535204.1:c.9690A= XP_011533506.1:p.Gln3230=
NM_000059.4:c.9786A= MANE Select NP_000050.3:p.Gln3262=