Canonical Allele Identifier: CA2082830191
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32396938T= , CM000675.2:g.32396938T= GRCh38
NC_000013.10:g.32971075T= , CM000675.1:g.32971075T= GRCh37
NC_000013.9:g.31869075T= NCBI36
NG_012772.3:g.86459T= , LRG_293:g.86459T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*65T= ENSP00000434898.2:n.*65T=
ENST00000528762.2:c.*909T= ENSP00000433168.2:n.*909T=
ENST00000530893.7:c.9173T= ENSP00000499438.2:p.Met3058=
ENST00000665585.2:c.*1104T= ENSP00000499570.2:n.*1104T=
ENST00000700202.2:c.9491T= ENSP00000514856.2:p.Met3164=
ENST00000700202.1:c.1958T= ENSP00000514856.1:p.Met653=
ENST00000700203.1:n.1669T=
ENST00000380152.8:c.9542T= MANE Select ENSP00000369497.3:p.Met3181=
ENST00000544455.6:c.9542T= ENSP00000439902.1:p.Met3181=
ENST00000614259.2:c.9550T= ENSP00000506251.1:n.9550T=
ENST00000665585.1:c.2420T=
ENST00000680887.1:c.9542T= ENSP00000505508.1:p.Met3181=
ENST00000380152.7:c.9542T= ENSP00000369497.3:p.Met3181=
ENST00000470094.1:c.625T=
ENST00000533776.1:n.130T=
ENST00000544455.5:c.9542T= ENSP00000439902.1:p.Met3181=
NM_000059.3:c.9542T= , LRG_293t1:c.9542T= NP_000050.2:p.Met3181=
XM_011535203.1:c.9542T= XP_011533505.1:p.Met3181=
XM_011535204.1:c.9446T= XP_011533506.1:p.Met3149=
NM_000059.4:c.9542T= MANE Select NP_000050.3:p.Met3181=