Canonical Allele Identifier: CA2082823156
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394795T= , CM000675.2:g.32394795T= GRCh38
NC_000013.10:g.32968932T= , CM000675.1:g.32968932T= GRCh37
NC_000013.9:g.31866932T= NCBI36
NG_012772.3:g.84316T= , LRG_293:g.84316T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.9363T= ENSP00000434898.2:p.Ala3121=
ENST00000528762.2:c.*730T= ENSP00000433168.2:n.*730T=
ENST00000530893.7:c.8994T= ENSP00000499438.2:p.Ala2998=
ENST00000665585.2:c.*925T= ENSP00000499570.2:n.*925T=
ENST00000666593.2:c.*208T= ENSP00000499256.2:n.*208T=
ENST00000700202.2:c.9312T= ENSP00000514856.2:p.Ala3104=
ENST00000700202.1:c.1779T= ENSP00000514856.1:p.Ala593=
ENST00000700203.1:n.1490T=
ENST00000380152.8:c.9363T= MANE Select ENSP00000369497.3:p.Ala3121=
ENST00000544455.6:c.9363T= ENSP00000439902.1:p.Ala3121=
ENST00000614259.2:c.9371T= ENSP00000506251.1:n.9371T=
ENST00000665585.1:c.2241T=
ENST00000666593.1:c.385T= ENSP00000499256.1:n.385T=
ENST00000680887.1:c.9363T= ENSP00000505508.1:p.Ala3121=
ENST00000380152.7:c.9363T= ENSP00000369497.3:p.Ala3121=
ENST00000470094.1:c.320T=
ENST00000544455.5:c.9363T= ENSP00000439902.1:p.Ala3121=
NM_000059.3:c.9363T= , LRG_293t1:c.9363T= NP_000050.2:p.Ala3121=
XM_011535203.1:c.9363T= XP_011533505.1:p.Ala3121=
XM_011535204.1:c.9267T= XP_011533506.1:p.Ala3089=
NM_000059.4:c.9363T= MANE Select NP_000050.3:p.Ala3121=