Canonical Allele Identifier: CA2082815999
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32371033_32371035delinsGGA , CM000675.2:g.32371033_32371035delinsGGA GRCh38
NC_000013.10:g.32945170_32945172delinsGGA , CM000675.1:g.32945170_32945172delinsGGA GRCh37
NC_000013.9:g.31843170_31843172delinsGGA NCBI36
NG_012772.3:g.60554_60556delinsGGA , LRG_293:g.60554_60556delinsGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8565_8567delinsGGA ENSP00000434898.2:p.Val2855=
ENST00000528762.2:c.8565_8567delinsGGA ENSP00000433168.2:p.Val2855=
ENST00000530893.7:c.8196_8198delinsGGA ENSP00000499438.2:p.Val2732=
ENST00000665585.2:c.8565_8567delinsGGA ENSP00000499570.2:p.Val2855=
ENST00000666593.2:c.8565_8567delinsGGA ENSP00000499256.2:p.Val2855=
ENST00000700202.2:c.8565_8567delinsGGA ENSP00000514856.2:p.Val2855=
ENST00000700202.1:c.1032_1034delinsGGA ENSP00000514856.1:p.Val344=
ENST00000380152.8:c.8565_8567delinsGGA MANE Select ENSP00000369497.3:p.Val2855=
ENST00000544455.6:c.8565_8567delinsGGA ENSP00000439902.1:p.Val2855=
ENST00000614259.2:c.8573_8575delinsGGA ENSP00000506251.1:n.8573_8575delinsGGA
ENST00000665585.1:c.1130_1132delinsGGA
ENST00000680887.1:c.8565_8567delinsGGA ENSP00000505508.1:p.Val2855=
ENST00000380152.7:c.8565_8567delinsGGA ENSP00000369497.3:p.Val2855=
ENST00000528762.1:c.63_65delinsGGA ENSP00000433168.1:p.Val21=
ENST00000544455.5:c.8565_8567delinsGGA ENSP00000439902.1:p.Val2855=
NM_000059.3:c.8565_8567delinsGGA , LRG_293t1:c.8565_8567delinsGGA NP_000050.2:p.Val2855=
XM_011535203.1:c.8565_8567delinsGGA XP_011533505.1:p.Val2855=
XM_011535204.1:c.8469_8471delinsGGA XP_011533506.1:p.Val2823=
XM_011535205.1:c.8565_8567delinsGGA XP_011533507.1:p.Val2855=
NM_000059.4:c.8565_8567delinsGGA MANE Select NP_000050.3:p.Val2855=