Canonical Allele Identifier: CA2082835806
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398408C= , CM000675.2:g.32398408C= GRCh38
NC_000013.10:g.32972545C= , CM000675.1:g.32972545C= GRCh37
NC_000013.9:g.31870545C= NCBI36
NG_012772.3:g.87929C= , LRG_293:g.87929C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*418C= ENSP00000434898.2:n.*418C=
ENST00000528762.2:c.*1262C= ENSP00000433168.2:n.*1262C=
ENST00000530893.7:c.9526C= ENSP00000499438.2:p.Gln3176=
ENST00000665585.2:c.*1457C= ENSP00000499570.2:n.*1457C=
ENST00000700202.2:c.9844C= ENSP00000514856.2:p.Gln3282=
ENST00000700202.1:c.2311C= ENSP00000514856.1:p.Gln771=
ENST00000700203.1:n.2022C=
ENST00000380152.8:c.9895C= MANE Select ENSP00000369497.3:p.Gln3299=
ENST00000544455.6:c.9895C= ENSP00000439902.1:p.Gln3299=
ENST00000614259.2:c.9903C= ENSP00000506251.1:n.9903C=
ENST00000680887.1:c.9895C= ENSP00000505508.1:p.Gln3299=
ENST00000380152.7:c.9895C= ENSP00000369497.3:p.Gln3299=
ENST00000533776.1:n.483C=
ENST00000544455.5:c.9895C= ENSP00000439902.1:p.Gln3299=
NM_000059.3:c.9895C= , LRG_293t1:c.9895C= NP_000050.2:p.Gln3299=
XM_011535203.1:c.9895C= XP_011533505.1:p.Gln3299=
XM_011535204.1:c.9799C= XP_011533506.1:p.Gln3267=
NM_000059.4:c.9895C= MANE Select NP_000050.3:p.Gln3299=