Canonical Allele Identifier: CA2082835179
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398302G= , CM000675.2:g.32398302G= GRCh38
NC_000013.10:g.32972439G= , CM000675.1:g.32972439G= GRCh37
NC_000013.9:g.31870439G= NCBI36
NG_012772.3:g.87823G= , LRG_293:g.87823G=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*312G= ENSP00000434898.2:n.*312G=
ENST00000528762.2:c.*1156G= ENSP00000433168.2:n.*1156G=
ENST00000530893.7:c.9420G= ENSP00000499438.2:p.Lys3140=
ENST00000665585.2:c.*1351G= ENSP00000499570.2:n.*1351G=
ENST00000700202.2:c.9738G= ENSP00000514856.2:p.Lys3246=
ENST00000700202.1:c.2205G= ENSP00000514856.1:p.Lys735=
ENST00000700203.1:n.1916G=
ENST00000380152.8:c.9789G= MANE Select ENSP00000369497.3:p.Lys3263=
ENST00000544455.6:c.9789G= ENSP00000439902.1:p.Lys3263=
ENST00000614259.2:c.9797G= ENSP00000506251.1:n.9797G=
ENST00000680887.1:c.9789G= ENSP00000505508.1:p.Lys3263=
ENST00000380152.7:c.9789G= ENSP00000369497.3:p.Lys3263=
ENST00000533776.1:n.377G=
ENST00000544455.5:c.9789G= ENSP00000439902.1:p.Lys3263=
NM_000059.3:c.9789G= , LRG_293t1:c.9789G= NP_000050.2:p.Lys3263=
XM_011535203.1:c.9789G= XP_011533505.1:p.Lys3263=
XM_011535204.1:c.9693G= XP_011533506.1:p.Lys3231=
NM_000059.4:c.9789G= MANE Select NP_000050.3:p.Lys3263=