Canonical Allele Identifier: CA2082833857
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398163T= , CM000675.2:g.32398163T= GRCh38
NC_000013.10:g.32972300T= , CM000675.1:g.32972300T= GRCh37
NC_000013.9:g.31870300T= NCBI36
NG_012772.3:g.87684T= , LRG_293:g.87684T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*173T= ENSP00000434898.2:n.*173T=
ENST00000528762.2:c.*1017T= ENSP00000433168.2:n.*1017T=
ENST00000530893.7:c.9281T= ENSP00000499438.2:p.Met3094=
ENST00000665585.2:c.*1212T= ENSP00000499570.2:n.*1212T=
ENST00000700202.2:c.9599T= ENSP00000514856.2:p.Met3200=
ENST00000700202.1:c.2066T= ENSP00000514856.1:p.Met689=
ENST00000700203.1:n.1777T=
ENST00000380152.8:c.9650T= MANE Select ENSP00000369497.3:p.Met3217=
ENST00000544455.6:c.9650T= ENSP00000439902.1:p.Met3217=
ENST00000614259.2:c.9658T= ENSP00000506251.1:n.9658T=
ENST00000665585.1:c.2528T=
ENST00000680887.1:c.9650T= ENSP00000505508.1:p.Met3217=
ENST00000380152.7:c.9650T= ENSP00000369497.3:p.Met3217=
ENST00000470094.1:c.733T=
ENST00000533776.1:n.238T=
ENST00000544455.5:c.9650T= ENSP00000439902.1:p.Met3217=
NM_000059.3:c.9650T= , LRG_293t1:c.9650T= NP_000050.2:p.Met3217=
XM_011535203.1:c.9650T= XP_011533505.1:p.Met3217=
XM_011535204.1:c.9554T= XP_011533506.1:p.Met3185=
NM_000059.4:c.9650T= MANE Select NP_000050.3:p.Met3217=