Canonical Allele Identifier: CA2082828139
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340200_32340201delinsGA , CM000675.2:g.32340200_32340201delinsGA GRCh38
NC_000013.10:g.32914337_32914338delinsGA , CM000675.1:g.32914337_32914338delinsGA GRCh37
NC_000013.9:g.31812337_31812338delinsGA NCBI36
NG_012772.3:g.29721_29722delinsGA , LRG_293:g.29721_29722delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.5845_5846delinsGA ENSP00000434898.2:p.Asp1949=
ENST00000528762.2:c.5845_5846delinsGA ENSP00000433168.2:p.Asp1949=
ENST00000530893.7:c.5476_5477delinsGA ENSP00000499438.2:p.Asp1826=
ENST00000665585.2:c.5845_5846delinsGA ENSP00000499570.2:p.Asp1949=
ENST00000666593.2:c.5845_5846delinsGA ENSP00000499256.2:p.Asp1949=
ENST00000700202.2:c.5845_5846delinsGA ENSP00000514856.2:p.Asp1949=
ENST00000380152.8:c.5845_5846delinsGA MANE Select ENSP00000369497.3:p.Asp1949=
ENST00000544455.6:c.5845_5846delinsGA ENSP00000439902.1:p.Asp1949=
ENST00000614259.2:c.5845_5846delinsGA ENSP00000506251.1:p.Asp1949=
ENST00000680887.1:c.5845_5846delinsGA ENSP00000505508.1:p.Asp1949=
ENST00000380152.7:c.5845_5846delinsGA ENSP00000369497.3:p.Asp1949=
ENST00000544455.5:c.5845_5846delinsGA ENSP00000439902.1:p.Asp1949=
ENST00000614259.1:n.5845_5846delinsGA
NM_000059.3:c.5845_5846delinsGA , LRG_293t1:c.5845_5846delinsGA NP_000050.2:p.Asp1949=
XM_011535203.1:c.5845_5846delinsGA XP_011533505.1:p.Asp1949=
XM_011535204.1:c.5845_5846delinsGA XP_011533506.1:p.Asp1949=
XM_011535205.1:c.5845_5846delinsGA XP_011533507.1:p.Asp1949=
NM_000059.4:c.5845_5846delinsGA MANE Select NP_000050.3:p.Asp1949=