Canonical Allele Identifier: CA2082830240
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32396943A= , CM000675.2:g.32396943A= GRCh38
NC_000013.10:g.32971080A= , CM000675.1:g.32971080A= GRCh37
NC_000013.9:g.31869080A= NCBI36
NG_012772.3:g.86464A= , LRG_293:g.86464A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*70A= ENSP00000434898.2:n.*70A=
ENST00000528762.2:c.*914A= ENSP00000433168.2:n.*914A=
ENST00000530893.7:c.9178A= ENSP00000499438.2:p.Ile3060=
ENST00000665585.2:c.*1109A= ENSP00000499570.2:n.*1109A=
ENST00000700202.2:c.9496A= ENSP00000514856.2:p.Ile3166=
ENST00000700202.1:c.1963A= ENSP00000514856.1:p.Ile655=
ENST00000700203.1:n.1674A=
ENST00000380152.8:c.9547A= MANE Select ENSP00000369497.3:p.Ile3183=
ENST00000544455.6:c.9547A= ENSP00000439902.1:p.Ile3183=
ENST00000614259.2:c.9555A= ENSP00000506251.1:n.9555A=
ENST00000665585.1:c.2425A=
ENST00000680887.1:c.9547A= ENSP00000505508.1:p.Ile3183=
ENST00000380152.7:c.9547A= ENSP00000369497.3:p.Ile3183=
ENST00000470094.1:c.630A=
ENST00000533776.1:n.135A=
ENST00000544455.5:c.9547A= ENSP00000439902.1:p.Ile3183=
NM_000059.3:c.9547A= , LRG_293t1:c.9547A= NP_000050.2:p.Ile3183=
XM_011535203.1:c.9547A= XP_011533505.1:p.Ile3183=
XM_011535204.1:c.9451A= XP_011533506.1:p.Ile3151=
NM_000059.4:c.9547A= MANE Select NP_000050.3:p.Ile3183=