Canonical Allele Identifier: CA2695199698
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2673995
ClinVar RCV Id: RCV003450596

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340762dup , CM000675.2:g.32340762dup GRCh38
NC_000013.10:g.32914899dup , CM000675.1:g.32914899dup GRCh37
NC_000013.9:g.31812899dup NCBI36
NG_012772.3:g.30283dup , LRG_293:g.30283dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.6407dup ENSP00000434898.2:p.Leu2136PhefsTer4
ENST00000528762.2:c.6407dup ENSP00000433168.2:p.Leu2136PhefsTer4
ENST00000530893.7:c.6038dup ENSP00000499438.2:p.Leu2013PhefsTer4
ENST00000665585.2:c.6407dup ENSP00000499570.2:p.Leu2136PhefsTer4
ENST00000666593.2:c.6407dup ENSP00000499256.2:p.Leu2136PhefsTer4
ENST00000700202.2:c.6407dup ENSP00000514856.2:p.Leu2136PhefsTer4
ENST00000380152.8:c.6407dup MANE Select ENSP00000369497.3:p.Leu2136PhefsTer4
ENST00000544455.6:c.6407dup ENSP00000439902.1:p.Leu2136PhefsTer4
ENST00000614259.2:c.6407dup ENSP00000506251.1:p.Leu2136PhefsTer4
ENST00000680887.1:c.6407dup ENSP00000505508.1:p.Leu2136PhefsTer4
ENST00000380152.7:c.6407dup ENSP00000369497.3:p.Leu2136PhefsTer4
ENST00000544455.5:c.6407dup ENSP00000439902.1:p.Leu2136PhefsTer4
ENST00000614259.1:n.6407dup
NM_000059.3:c.6407dup , LRG_293t1:c.6407dup NP_000050.2:p.Leu2136PhefsTer4
XM_011535203.1:c.6407dup XP_011533505.1:p.Leu2136PhefsTer4
XM_011535204.1:c.6407dup XP_011533506.1:p.Leu2136PhefsTer4
XM_011535205.1:c.6407dup XP_011533507.1:p.Leu2136PhefsTer4
NM_000059.4:c.6407dup MANE Select NP_000050.3:p.Leu2136PhefsTer4