Canonical Allele Identifier: CA2082827868
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32376646_32376649delinsTTAA , CM000675.2:g.32376646_32376649delinsTTAA GRCh38
NC_000013.10:g.32950783_32950786delinsTTAA , CM000675.1:g.32950783_32950786delinsTTAA GRCh37
NC_000013.9:g.31848783_31848786delinsTTAA NCBI36
NG_012772.3:g.66167_66170delinsTTAA , LRG_293:g.66167_66170delinsTTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8633-24_8633-21delinsTTAA ENSP00000434898.2:n.8633-24_8633-21delinsTTAA
ENST00000528762.2:c.8697-24_8697-21delinsTTAA ENSP00000433168.2:n.8697-24_8697-21delinsTTAA
ENST00000530893.7:c.8264-24_8264-21delinsTTAA ENSP00000499438.2:n.8264-24_8264-21delinsTTAA
ENST00000665585.2:c.*195-24_*195-21delinsTTAA ENSP00000499570.2:n.*195-24_*195-21delinsTTAA
ENST00000666593.2:c.8633-24_8633-21delinsTTAA ENSP00000499256.2:n.8633-24_8633-21delinsTTAA
ENST00000700202.2:c.8633-24_8633-21delinsTTAA ENSP00000514856.2:n.8633-24_8633-21delinsTTAA
ENST00000700202.1:c.1100-24_1100-21delinsTTAA ENSP00000514856.1:n.1100-24_1100-21delinsTTAA
ENST00000700203.1:n.736_739delinsTTAA
ENST00000380152.8:c.8633-24_8633-21delinsTTAA MANE Select ENSP00000369497.3:n.8633-24_8633-21delinsTTAA
ENST00000544455.6:c.8633-24_8633-21delinsTTAA ENSP00000439902.1:n.8633-24_8633-21delinsTTAA
ENST00000614259.2:c.8641-24_8641-21delinsTTAA ENSP00000506251.1:n.8641-24_8641-21delinsTTAA
ENST00000665585.1:c.1511-24_1511-21delinsTTAA
ENST00000680887.1:c.8633-24_8633-21delinsTTAA ENSP00000505508.1:n.8633-24_8633-21delinsTTAA
ENST00000380152.7:c.8633-24_8633-21delinsTTAA ENSP00000369497.3:n.8633-24_8633-21delinsTTAA
ENST00000528762.1:c.195-24_195-21delinsTTAA ENSP00000433168.1:n.195-24_195-21delinsTTAA
ENST00000544455.5:c.8633-24_8633-21delinsTTAA ENSP00000439902.1:n.8633-24_8633-21delinsTTAA
NM_000059.3:c.8633-24_8633-21delinsTTAA , LRG_293t1:c.8633-24_8633-21delinsTTAA NP_000050.2:n.8633-24_8633-21delinsTTAA
XM_011535203.1:c.8633-24_8633-21delinsTTAA XP_011533505.1:n.8633-24_8633-21delinsTTAA
XM_011535204.1:c.8537-24_8537-21delinsTTAA XP_011533506.1:n.8537-24_8537-21delinsTTAA
XM_011535205.1:c.8633-24_8633-21delinsTTAA XP_011533507.1:n.8633-24_8633-21delinsTTAA
NM_000059.4:c.8633-24_8633-21delinsTTAA MANE Select NP_000050.3:n.8633-24_8633-21delinsTTAA