Canonical Allele Identifier: CA2082772727
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32315573_32315581delinsGTCGCCGCC , CM000675.2:g.32315573_32315581delinsGTCGCCGCC GRCh38
NC_000013.10:g.32889710_32889718delinsGTCGCCGCC , CM000675.1:g.32889710_32889718delinsGTCGCCGCC GRCh37
NC_000013.9:g.31787710_31787718delinsGTCGCCGCC NCBI36
NG_012772.3:g.5094_5102delinsGTCGCCGCC , LRG_293:g.5094_5102delinsGTCGCCGCC
NG_017006.1:g.1374_1382delinsGGCGGCGAC
NG_017006.2:g.4783_4791delinsGGCGGCGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.-134_-126delinsGTCGCCGCC ENSP00000434898.2:n.-134_-126delinsGTCGCCGCC
ENST00000528762.2:c.-134_-126delinsGTCGCCGCC ENSP00000433168.2:n.-134_-126delinsGTCGCCGCC
ENST00000530893.7:c.-499_-491delinsGTCGCCGCC ENSP00000499438.2:n.-499_-491delinsGTCGCCGCC
ENST00000665585.2:c.-134_-126delinsGTCGCCGCC ENSP00000499570.2:n.-134_-126delinsGTCGCCGCC
ENST00000666593.2:c.-134_-126delinsGTCGCCGCC ENSP00000499256.2:n.-134_-126delinsGTCGCCGCC
ENST00000700202.2:c.-134_-126delinsGTCGCCGCC ENSP00000514856.2:n.-134_-126delinsGTCGCCGCC
ENST00000380152.8:c.-134_-126delinsGTCGCCGCC MANE Select ENSP00000369497.3:n.-134_-126delinsGTCGCCGCC
ENST00000544455.6:c.-40+428_-40+436delinsGTCGCCGCC ENSP00000439902.1:n.-40+428_-40+436delinsGTCGCCGCC
ENST00000380152.7:c.-134_-126delinsGTCGCCGCC ENSP00000369497.3:n.-134_-126delinsGTCGCCGCC
ENST00000530893.6:n.69_77delinsGTCGCCGCC
ENST00000544455.5:c.-134_-126delinsGTCGCCGCC ENSP00000439902.1:n.-134_-126delinsGTCGCCGCC
NM_000059.3:c.-134_-126delinsGTCGCCGCC , LRG_293t1:c.-134_-126delinsGTCGCCGCC NP_000050.2:n.-134_-126delinsGTCGCCGCC
XM_011535203.1:c.-40+428_-40+436delinsGTCGCCGCC XP_011533505.1:n.-40+428_-40+436delinsGTCGCCGCC
XM_011535204.1:c.-134_-126delinsGTCGCCGCC XP_011533506.1:n.-134_-126delinsGTCGCCGCC
XM_011535205.1:c.-134_-126delinsGTCGCCGCC XP_011533507.1:n.-134_-126delinsGTCGCCGCC
NM_000059.4:c.-134_-126delinsGTCGCCGCC MANE Select NP_000050.3:n.-134_-126delinsGTCGCCGCC