Canonical Allele Identifier: CA2082835807
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398409A= , CM000675.2:g.32398409A= GRCh38
NC_000013.10:g.32972546A= , CM000675.1:g.32972546A= GRCh37
NC_000013.9:g.31870546A= NCBI36
NG_012772.3:g.87930A= , LRG_293:g.87930A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*419A= ENSP00000434898.2:n.*419A=
ENST00000528762.2:c.*1263A= ENSP00000433168.2:n.*1263A=
ENST00000530893.7:c.9527A= ENSP00000499438.2:p.Gln3176=
ENST00000665585.2:c.*1458A= ENSP00000499570.2:n.*1458A=
ENST00000700202.2:c.9845A= ENSP00000514856.2:p.Gln3282=
ENST00000700202.1:c.2312A= ENSP00000514856.1:p.Gln771=
ENST00000700203.1:n.2023A=
ENST00000380152.8:c.9896A= MANE Select ENSP00000369497.3:p.Gln3299=
ENST00000544455.6:c.9896A= ENSP00000439902.1:p.Gln3299=
ENST00000614259.2:c.9904A= ENSP00000506251.1:n.9904A=
ENST00000680887.1:c.9896A= ENSP00000505508.1:p.Gln3299=
ENST00000380152.7:c.9896A= ENSP00000369497.3:p.Gln3299=
ENST00000533776.1:n.484A=
ENST00000544455.5:c.9896A= ENSP00000439902.1:p.Gln3299=
NM_000059.3:c.9896A= , LRG_293t1:c.9896A= NP_000050.2:p.Gln3299=
XM_011535203.1:c.9896A= XP_011533505.1:p.Gln3299=
XM_011535204.1:c.9800A= XP_011533506.1:p.Gln3267=
NM_000059.4:c.9896A= MANE Select NP_000050.3:p.Gln3299=