Canonical Allele Identifier: CA2082835136
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398297_32398298delinsCA , CM000675.2:g.32398297_32398298delinsCA GRCh38
NC_000013.10:g.32972434_32972435delinsCA , CM000675.1:g.32972434_32972435delinsCA GRCh37
NC_000013.9:g.31870434_31870435delinsCA NCBI36
NG_012772.3:g.87818_87819delinsCA , LRG_293:g.87818_87819delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*307_*308delinsCA ENSP00000434898.2:n.*307_*308delinsCA
ENST00000528762.2:c.*1151_*1152delinsCA ENSP00000433168.2:n.*1151_*1152delinsCA
ENST00000530893.7:c.9415_9416delinsCA ENSP00000499438.2:p.Gln3139=
ENST00000665585.2:c.*1346_*1347delinsCA ENSP00000499570.2:n.*1346_*1347delinsCA
ENST00000700202.2:c.9733_9734delinsCA ENSP00000514856.2:p.Gln3245=
ENST00000700202.1:c.2200_2201delinsCA ENSP00000514856.1:p.Gln734=
ENST00000700203.1:n.1911_1912delinsCA
ENST00000380152.8:c.9784_9785delinsCA MANE Select ENSP00000369497.3:p.Gln3262=
ENST00000544455.6:c.9784_9785delinsCA ENSP00000439902.1:p.Gln3262=
ENST00000614259.2:c.9792_9793delinsCA ENSP00000506251.1:n.9792_9793delinsCA
ENST00000680887.1:c.9784_9785delinsCA ENSP00000505508.1:p.Gln3262=
ENST00000380152.7:c.9784_9785delinsCA ENSP00000369497.3:p.Gln3262=
ENST00000533776.1:n.372_373delinsCA
ENST00000544455.5:c.9784_9785delinsCA ENSP00000439902.1:p.Gln3262=
NM_000059.3:c.9784_9785delinsCA , LRG_293t1:c.9784_9785delinsCA NP_000050.2:p.Gln3262=
XM_011535203.1:c.9784_9785delinsCA XP_011533505.1:p.Gln3262=
XM_011535204.1:c.9688_9689delinsCA XP_011533506.1:p.Gln3230=
NM_000059.4:c.9784_9785delinsCA MANE Select NP_000050.3:p.Gln3262=