Canonical Allele Identifier: CA2082822488
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394737C= , CM000675.2:g.32394737C= GRCh38
NC_000013.10:g.32968874C= , CM000675.1:g.32968874C= GRCh37
NC_000013.9:g.31866874C= NCBI36
NG_012772.3:g.84258C= , LRG_293:g.84258C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.9305C= ENSP00000434898.2:p.Ala3102=
ENST00000528762.2:c.*672C= ENSP00000433168.2:n.*672C=
ENST00000530893.7:c.8936C= ENSP00000499438.2:p.Ala2979=
ENST00000665585.2:c.*867C= ENSP00000499570.2:n.*867C=
ENST00000666593.2:c.*150C= ENSP00000499256.2:n.*150C=
ENST00000700202.2:c.9254C= ENSP00000514856.2:p.Ala3085=
ENST00000700202.1:c.1721C= ENSP00000514856.1:p.Ala574=
ENST00000700203.1:n.1432C=
ENST00000380152.8:c.9305C= MANE Select ENSP00000369497.3:p.Ala3102=
ENST00000544455.6:c.9305C= ENSP00000439902.1:p.Ala3102=
ENST00000614259.2:c.9313C= ENSP00000506251.1:n.9313C=
ENST00000665585.1:c.2183C=
ENST00000666593.1:c.327C= ENSP00000499256.1:n.327C=
ENST00000680887.1:c.9305C= ENSP00000505508.1:p.Ala3102=
ENST00000380152.7:c.9305C= ENSP00000369497.3:p.Ala3102=
ENST00000470094.1:c.262C=
ENST00000544455.5:c.9305C= ENSP00000439902.1:p.Ala3102=
NM_000059.3:c.9305C= , LRG_293t1:c.9305C= NP_000050.2:p.Ala3102=
XM_011535203.1:c.9305C= XP_011533505.1:p.Ala3102=
XM_011535204.1:c.9209C= XP_011533506.1:p.Ala3070=
NM_000059.4:c.9305C= MANE Select NP_000050.3:p.Ala3102=