Canonical Allele Identifier: CA2082835507
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398356A= , CM000675.2:g.32398356A= GRCh38
NC_000013.10:g.32972493A= , CM000675.1:g.32972493A= GRCh37
NC_000013.9:g.31870493A= NCBI36
NG_012772.3:g.87877A= , LRG_293:g.87877A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*366A= ENSP00000434898.2:n.*366A=
ENST00000528762.2:c.*1210A= ENSP00000433168.2:n.*1210A=
ENST00000530893.7:c.9474A= ENSP00000499438.2:p.Pro3158=
ENST00000665585.2:c.*1405A= ENSP00000499570.2:n.*1405A=
ENST00000700202.2:c.9792A= ENSP00000514856.2:p.Pro3264=
ENST00000700202.1:c.2259A= ENSP00000514856.1:p.Pro753=
ENST00000700203.1:n.1970A=
ENST00000380152.8:c.9843A= MANE Select ENSP00000369497.3:p.Pro3281=
ENST00000544455.6:c.9843A= ENSP00000439902.1:p.Pro3281=
ENST00000614259.2:c.9851A= ENSP00000506251.1:n.9851A=
ENST00000680887.1:c.9843A= ENSP00000505508.1:p.Pro3281=
ENST00000380152.7:c.9843A= ENSP00000369497.3:p.Pro3281=
ENST00000533776.1:n.431A=
ENST00000544455.5:c.9843A= ENSP00000439902.1:p.Pro3281=
NM_000059.3:c.9843A= , LRG_293t1:c.9843A= NP_000050.2:p.Pro3281=
XM_011535203.1:c.9843A= XP_011533505.1:p.Pro3281=
XM_011535204.1:c.9747A= XP_011533506.1:p.Pro3249=
NM_000059.4:c.9843A= MANE Select NP_000050.3:p.Pro3281=