Canonical Allele Identifier: CA2082834118
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398194A= , CM000675.2:g.32398194A= GRCh38
NC_000013.10:g.32972331A= , CM000675.1:g.32972331A= GRCh37
NC_000013.9:g.31870331A= NCBI36
NG_012772.3:g.87715A= , LRG_293:g.87715A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*204A= ENSP00000434898.2:n.*204A=
ENST00000528762.2:c.*1048A= ENSP00000433168.2:n.*1048A=
ENST00000530893.7:c.9312A= ENSP00000499438.2:p.Gln3104=
ENST00000665585.2:c.*1243A= ENSP00000499570.2:n.*1243A=
ENST00000700202.2:c.9630A= ENSP00000514856.2:p.Gln3210=
ENST00000700202.1:c.2097A= ENSP00000514856.1:p.Gln699=
ENST00000700203.1:n.1808A=
ENST00000380152.8:c.9681A= MANE Select ENSP00000369497.3:p.Gln3227=
ENST00000544455.6:c.9681A= ENSP00000439902.1:p.Gln3227=
ENST00000614259.2:c.9689A= ENSP00000506251.1:n.9689A=
ENST00000665585.1:c.2559A=
ENST00000680887.1:c.9681A= ENSP00000505508.1:p.Gln3227=
ENST00000380152.7:c.9681A= ENSP00000369497.3:p.Gln3227=
ENST00000470094.1:c.764A=
ENST00000533776.1:n.269A=
ENST00000544455.5:c.9681A= ENSP00000439902.1:p.Gln3227=
NM_000059.3:c.9681A= , LRG_293t1:c.9681A= NP_000050.2:p.Gln3227=
XM_011535203.1:c.9681A= XP_011533505.1:p.Gln3227=
XM_011535204.1:c.9585A= XP_011533506.1:p.Gln3195=
NM_000059.4:c.9681A= MANE Select NP_000050.3:p.Gln3227=