Canonical Allele Identifier: CA2082814222
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32370530_32370533delinsAATT , CM000675.2:g.32370530_32370533delinsAATT GRCh38
NC_000013.10:g.32944667_32944670delinsAATT , CM000675.1:g.32944667_32944670delinsAATT GRCh37
NC_000013.9:g.31842667_31842670delinsAATT NCBI36
NG_012772.3:g.60051_60054delinsAATT , LRG_293:g.60051_60054delinsAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8460_8463delinsAATT ENSP00000434898.2:p.Val2820=
ENST00000528762.2:c.8460_8463delinsAATT ENSP00000433168.2:p.Val2820=
ENST00000530893.7:c.8091_8094delinsAATT ENSP00000499438.2:p.Val2697=
ENST00000665585.2:c.8460_8463delinsAATT ENSP00000499570.2:p.Val2820=
ENST00000666593.2:c.8460_8463delinsAATT ENSP00000499256.2:p.Val2820=
ENST00000700202.2:c.8460_8463delinsAATT ENSP00000514856.2:p.Val2820=
ENST00000700202.1:c.927_930delinsAATT ENSP00000514856.1:p.Val309=
ENST00000380152.8:c.8460_8463delinsAATT MANE Select ENSP00000369497.3:p.Val2820=
ENST00000544455.6:c.8460_8463delinsAATT ENSP00000439902.1:p.Val2820=
ENST00000614259.2:c.8468_8471delinsAATT ENSP00000506251.1:n.8468_8471delinsAATT
ENST00000665585.1:c.1025_1028delinsAATT
ENST00000680887.1:c.8460_8463delinsAATT ENSP00000505508.1:p.Val2820=
ENST00000380152.7:c.8460_8463delinsAATT ENSP00000369497.3:p.Val2820=
ENST00000544455.5:c.8460_8463delinsAATT ENSP00000439902.1:p.Val2820=
NM_000059.3:c.8460_8463delinsAATT , LRG_293t1:c.8460_8463delinsAATT NP_000050.2:p.Val2820=
XM_011535203.1:c.8460_8463delinsAATT XP_011533505.1:p.Val2820=
XM_011535204.1:c.8364_8367delinsAATT XP_011533506.1:p.Val2788=
XM_011535205.1:c.8460_8463delinsAATT XP_011533507.1:p.Val2820=
NM_000059.4:c.8460_8463delinsAATT MANE Select NP_000050.3:p.Val2820=