Canonical Allele Identifier: CA2082833935
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398175A= , CM000675.2:g.32398175A= GRCh38
NC_000013.10:g.32972312A= , CM000675.1:g.32972312A= GRCh37
NC_000013.9:g.31870312A= NCBI36
NG_012772.3:g.87696A= , LRG_293:g.87696A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*185A= ENSP00000434898.2:n.*185A=
ENST00000528762.2:c.*1029A= ENSP00000433168.2:n.*1029A=
ENST00000530893.7:c.9293A= ENSP00000499438.2:p.Asn3098=
ENST00000665585.2:c.*1224A= ENSP00000499570.2:n.*1224A=
ENST00000700202.2:c.9611A= ENSP00000514856.2:p.Asn3204=
ENST00000700202.1:c.2078A= ENSP00000514856.1:p.Asn693=
ENST00000700203.1:n.1789A=
ENST00000380152.8:c.9662A= MANE Select ENSP00000369497.3:p.Asn3221=
ENST00000544455.6:c.9662A= ENSP00000439902.1:p.Asn3221=
ENST00000614259.2:c.9670A= ENSP00000506251.1:n.9670A=
ENST00000665585.1:c.2540A=
ENST00000680887.1:c.9662A= ENSP00000505508.1:p.Asn3221=
ENST00000380152.7:c.9662A= ENSP00000369497.3:p.Asn3221=
ENST00000470094.1:c.745A=
ENST00000533776.1:n.250A=
ENST00000544455.5:c.9662A= ENSP00000439902.1:p.Asn3221=
NM_000059.3:c.9662A= , LRG_293t1:c.9662A= NP_000050.2:p.Asn3221=
XM_011535203.1:c.9662A= XP_011533505.1:p.Asn3221=
XM_011535204.1:c.9566A= XP_011533506.1:p.Asn3189=
NM_000059.4:c.9662A= MANE Select NP_000050.3:p.Asn3221=