Canonical Allele Identifier: CA2082831161
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32397063A= , CM000675.2:g.32397063A= GRCh38
NC_000013.10:g.32971200A= , CM000675.1:g.32971200A= GRCh37
NC_000013.9:g.31869200A= NCBI36
NG_012772.3:g.86584A= , LRG_293:g.86584A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*171+19A= ENSP00000434898.2:n.*171+19A=
ENST00000528762.2:c.*1015+19A= ENSP00000433168.2:n.*1015+19A=
ENST00000530893.7:c.9279+19A= ENSP00000499438.2:n.9279+19A=
ENST00000665585.2:c.*1210+19A= ENSP00000499570.2:n.*1210+19A=
ENST00000700202.2:c.9597+19A= ENSP00000514856.2:n.9597+19A=
ENST00000700202.1:c.2064+19A= ENSP00000514856.1:n.2064+19A=
ENST00000700203.1:n.1775+19A=
ENST00000380152.8:c.9648+19A= MANE Select ENSP00000369497.3:n.9648+19A=
ENST00000544455.6:c.9648+19A= ENSP00000439902.1:n.9648+19A=
ENST00000614259.2:c.9656+19A= ENSP00000506251.1:n.9656+19A=
ENST00000665585.1:c.2526+19A=
ENST00000680887.1:c.9648+19A= ENSP00000505508.1:n.9648+19A=
ENST00000380152.7:c.9648+19A= ENSP00000369497.3:n.9648+19A=
ENST00000470094.1:c.731+19A=
ENST00000533776.1:n.236+19A=
ENST00000544455.5:c.9648+19A= ENSP00000439902.1:n.9648+19A=
NM_000059.3:c.9648+19A= , LRG_293t1:c.9648+19A= NP_000050.2:n.9648+19A=
XM_011535203.1:c.9648+19A= XP_011533505.1:n.9648+19A=
XM_011535204.1:c.9552+19A= XP_011533506.1:n.9552+19A=
NM_000059.4:c.9648+19A= MANE Select NP_000050.3:n.9648+19A=