Canonical Allele Identifier: CA2082836148
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379445_32379510delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA , CM000675.2:g.32379445_32379510delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA GRCh38
NC_000013.10:g.32953582_32953647delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA , CM000675.1:g.32953582_32953647delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA GRCh37
NC_000013.9:g.31851582_31851647delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA NCBI36
NG_012772.3:g.68966_69031delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA , LRG_293:g.68966_69031delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000434898.2:p.Gly2961=
ENST00000528762.2:c.*250_*315delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000433168.2:n.*250_*315delinsTTTATC...
ENST00000530893.7:c.8514_8579delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000499438.2:p.Gly2838=
ENST00000665585.2:c.*445_*510delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000499570.2:n.*445_*510delinsTTTATC...
ENST00000666593.2:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000499256.2:p.Gly2961=
ENST00000700202.2:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000514856.2:p.Gly2961=
ENST00000700202.1:c.1350_1415delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000514856.1:p.Gly450=
ENST00000700203.1:n.1010_1075delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA
ENST00000380152.8:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA MANE Select ENSP00000369497.3:p.Gly2961=
ENST00000544455.6:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000439902.1:p.Gly2961=
ENST00000614259.2:c.8891_8956delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000506251.1:n.8891_8956delinsTTTATC...
ENST00000665585.1:c.1761_1826delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA
ENST00000680887.1:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000505508.1:p.Gly2961=
ENST00000380152.7:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000369497.3:p.Gly2961=
ENST00000544455.5:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA ENSP00000439902.1:p.Gly2961=
NM_000059.3:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA , LRG_293t1:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA NP_000050.2:p.Gly2961=
XM_011535203.1:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA XP_011533505.1:p.Gly2961=
XM_011535204.1:c.8787_8852delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA XP_011533506.1:p.Gly2929=
XM_011535205.1:c.8755-305_8755-240delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA XP_011533507.1:n.8755-305_8755-240delinsT...
NM_000059.4:c.8883_8948delinsTTTATCAAGGGATGTCACAACCGTGTGGAAGTTGCGTATTGTAAGCTATTCAAAAAAAGAAAAAGA MANE Select NP_000050.3:p.Gly2961=