Canonical Allele Identifier: CA2082815459
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356586_32356600delinsCCCTCTGCGTGTTCT , CM000675.2:g.32356586_32356600delinsCCCTCTGCGTGTTCT GRCh38
NC_000013.10:g.32930723_32930737delinsCCCTCTGCGTGTTCT , CM000675.1:g.32930723_32930737delinsCCCTCTGCGTGTTCT GRCh37
NC_000013.9:g.31828723_31828737delinsCCCTCTGCGTGTTCT NCBI36
NG_012772.3:g.46107_46121delinsCCCTCTGCGTGTTCT , LRG_293:g.46107_46121delinsCCCTCTGCGTGTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000434898.2:p.Pro2532=
ENST00000528762.2:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000433168.2:p.Pro2532=
ENST00000530893.7:c.7225_7239delinsCCCTCTGCGTGTTCT ENSP00000499438.2:p.Pro2409=
ENST00000665585.2:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000499570.2:p.Pro2532=
ENST00000666593.2:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000499256.2:p.Pro2532=
ENST00000700202.2:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000514856.2:p.Pro2532=
ENST00000700202.1:c.61_75delinsCCCTCTGCGTGTTCT ENSP00000514856.1:p.Pro21=
ENST00000380152.8:c.7594_7608delinsCCCTCTGCGTGTTCT MANE Select ENSP00000369497.3:p.Pro2532=
ENST00000544455.6:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000439902.1:p.Pro2532=
ENST00000614259.2:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000506251.1:p.Pro2532=
ENST00000665585.1:c.159_173delinsCCCTCTGCGTGTTCT
ENST00000680887.1:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000505508.1:p.Pro2532=
ENST00000380152.7:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000369497.3:p.Pro2532=
ENST00000544455.5:c.7594_7608delinsCCCTCTGCGTGTTCT ENSP00000439902.1:p.Pro2532=
ENST00000614259.1:n.7594_7608delinsCCCTCTGCGTGTTCT
NM_000059.3:c.7594_7608delinsCCCTCTGCGTGTTCT , LRG_293t1:c.7594_7608delinsCCCTCTGCGTGTTCT NP_000050.2:p.Pro2532=
XM_011535203.1:c.7594_7608delinsCCCTCTGCGTGTTCT XP_011533505.1:p.Pro2532=
XM_011535204.1:c.7498_7512delinsCCCTCTGCGTGTTCT XP_011533506.1:p.Pro2500=
XM_011535205.1:c.7594_7608delinsCCCTCTGCGTGTTCT XP_011533507.1:p.Pro2532=
NM_000059.4:c.7594_7608delinsCCCTCTGCGTGTTCT MANE Select NP_000050.3:p.Pro2532=