Canonical Allele Identifier: CA2082777476
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32316744_32316745delinsTA , CM000675.2:g.32316744_32316745delinsTA GRCh38
NC_000013.10:g.32890881_32890882delinsTA , CM000675.1:g.32890881_32890882delinsTA GRCh37
NC_000013.9:g.31788881_31788882delinsTA NCBI36
NG_012772.3:g.6265_6266delinsTA , LRG_293:g.6265_6266delinsTA
NG_017006.1:g.210_211delinsTA
NG_017006.2:g.3619_3620delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.67+217_67+218delinsTA ENSP00000434898.2:n.67+217_67+218delinsTA
ENST00000528762.2:c.67+217_67+218delinsTA ENSP00000433168.2:n.67+217_67+218delinsTA
ENST00000530893.7:c.-303+221_-303+222delinsTA ENSP00000499438.2:n.-303+221_-303+222delinsTA
ENST00000665585.2:c.67+217_67+218delinsTA ENSP00000499570.2:n.67+217_67+218delinsTA
ENST00000666593.2:c.67+217_67+218delinsTA ENSP00000499256.2:n.67+217_67+218delinsTA
ENST00000700202.2:c.67+217_67+218delinsTA ENSP00000514856.2:n.67+217_67+218delinsTA
ENST00000700199.1:n.408_409delinsTA
ENST00000700200.1:n.191+217_191+218delinsTA
ENST00000700201.1:c.67+217_67+218delinsTA ENSP00000514855.1:n.67+217_67+218delinsTA
ENST00000380152.8:c.67+217_67+218delinsTA MANE Select ENSP00000369497.3:n.67+217_67+218delinsTA
ENST00000544455.6:c.67+217_67+218delinsTA ENSP00000439902.1:n.67+217_67+218delinsTA
ENST00000614259.2:c.67+217_67+218delinsTA ENSP00000506251.1:n.67+217_67+218delinsTA
ENST00000680887.1:c.67+217_67+218delinsTA ENSP00000505508.1:n.67+217_67+218delinsTA
ENST00000380152.7:c.67+217_67+218delinsTA ENSP00000369497.3:n.67+217_67+218delinsTA
ENST00000530893.6:n.265+221_265+222delinsTA
ENST00000544455.5:c.67+217_67+218delinsTA ENSP00000439902.1:n.67+217_67+218delinsTA
ENST00000614259.1:n.67+217_67+218delinsTA
NM_000059.3:c.67+217_67+218delinsTA , LRG_293t1:c.67+217_67+218delinsTA NP_000050.2:n.67+217_67+218delinsTA
XM_011535203.1:c.67+217_67+218delinsTA XP_011533505.1:n.67+217_67+218delinsTA
XM_011535204.1:c.67+217_67+218delinsTA XP_011533506.1:n.67+217_67+218delinsTA
XM_011535205.1:c.67+217_67+218delinsTA XP_011533507.1:n.67+217_67+218delinsTA
NM_000059.4:c.67+217_67+218delinsTA MANE Select NP_000050.3:n.67+217_67+218delinsTA