Canonical Allele Identifier: CA2082831177
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32397071T= , CM000675.2:g.32397071T= GRCh38
NC_000013.10:g.32971208T= , CM000675.1:g.32971208T= GRCh37
NC_000013.9:g.31869208T= NCBI36
NG_012772.3:g.86592T= , LRG_293:g.86592T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*171+27T= ENSP00000434898.2:n.*171+27T=
ENST00000528762.2:c.*1015+27T= ENSP00000433168.2:n.*1015+27T=
ENST00000530893.7:c.9279+27T= ENSP00000499438.2:n.9279+27T=
ENST00000665585.2:c.*1210+27T= ENSP00000499570.2:n.*1210+27T=
ENST00000700202.2:c.9597+27T= ENSP00000514856.2:n.9597+27T=
ENST00000700202.1:c.2064+27T= ENSP00000514856.1:n.2064+27T=
ENST00000700203.1:n.1775+27T=
ENST00000380152.8:c.9648+27T= MANE Select ENSP00000369497.3:n.9648+27T=
ENST00000544455.6:c.9648+27T= ENSP00000439902.1:n.9648+27T=
ENST00000614259.2:c.9656+27T= ENSP00000506251.1:n.9656+27T=
ENST00000665585.1:c.2526+27T=
ENST00000680887.1:c.9648+27T= ENSP00000505508.1:n.9648+27T=
ENST00000380152.7:c.9648+27T= ENSP00000369497.3:n.9648+27T=
ENST00000470094.1:c.731+27T=
ENST00000533776.1:n.236+27T=
ENST00000544455.5:c.9648+27T= ENSP00000439902.1:n.9648+27T=
NM_000059.3:c.9648+27T= , LRG_293t1:c.9648+27T= NP_000050.2:n.9648+27T=
XM_011535203.1:c.9648+27T= XP_011533505.1:n.9648+27T=
XM_011535204.1:c.9552+27T= XP_011533506.1:n.9552+27T=
NM_000059.4:c.9648+27T= MANE Select NP_000050.3:n.9648+27T=