Canonical Allele Identifier: CA2082833967
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398178G= , CM000675.2:g.32398178G= GRCh38
NC_000013.10:g.32972315G= , CM000675.1:g.32972315G= GRCh37
NC_000013.9:g.31870315G= NCBI36
NG_012772.3:g.87699G= , LRG_293:g.87699G=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*188G= ENSP00000434898.2:n.*188G=
ENST00000528762.2:c.*1032G= ENSP00000433168.2:n.*1032G=
ENST00000530893.7:c.9296G= ENSP00000499438.2:p.Cys3099=
ENST00000665585.2:c.*1227G= ENSP00000499570.2:n.*1227G=
ENST00000700202.2:c.9614G= ENSP00000514856.2:p.Cys3205=
ENST00000700202.1:c.2081G= ENSP00000514856.1:p.Cys694=
ENST00000700203.1:n.1792G=
ENST00000380152.8:c.9665G= MANE Select ENSP00000369497.3:p.Cys3222=
ENST00000544455.6:c.9665G= ENSP00000439902.1:p.Cys3222=
ENST00000614259.2:c.9673G= ENSP00000506251.1:n.9673G=
ENST00000665585.1:c.2543G=
ENST00000680887.1:c.9665G= ENSP00000505508.1:p.Cys3222=
ENST00000380152.7:c.9665G= ENSP00000369497.3:p.Cys3222=
ENST00000470094.1:c.748G=
ENST00000533776.1:n.253G=
ENST00000544455.5:c.9665G= ENSP00000439902.1:p.Cys3222=
NM_000059.3:c.9665G= , LRG_293t1:c.9665G= NP_000050.2:p.Cys3222=
XM_011535203.1:c.9665G= XP_011533505.1:p.Cys3222=
XM_011535204.1:c.9569G= XP_011533506.1:p.Cys3190=
NM_000059.4:c.9665G= MANE Select NP_000050.3:p.Cys3222=