Canonical Allele Identifier: CA387760216
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431189
ClinVar RCV Id: RCV000496918
dbSNP Id: rs1135401831

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32331018G>C , CM000675.2:g.32331018G>C GRCh38
NC_000013.10:g.32905155G>C , CM000675.1:g.32905155G>C GRCh37
NC_000013.9:g.31803155G>C NCBI36
NG_012772.3:g.20539G>C , LRG_293:g.20539G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.781G>C ENSP00000434898.2:p.Ala261Pro
ENST00000528762.2:c.781G>C ENSP00000433168.2:p.Ala261Pro
ENST00000530893.7:c.412G>C ENSP00000499438.2:p.Ala138Pro
ENST00000665585.2:c.781G>C ENSP00000499570.2:p.Ala261Pro
ENST00000666593.2:c.781G>C ENSP00000499256.2:p.Ala261Pro
ENST00000700202.2:c.781G>C ENSP00000514856.2:p.Ala261Pro
ENST00000700201.1:c.*560G>C ENSP00000514855.1:n.*560G>C
ENST00000380152.8:c.781G>C MANE Select ENSP00000369497.3:p.Ala261Pro
ENST00000544455.6:c.781G>C ENSP00000439902.1:p.Ala261Pro
ENST00000614259.2:c.781G>C ENSP00000506251.1:p.Ala261Pro
ENST00000680887.1:c.781G>C ENSP00000505508.1:p.Ala261Pro
ENST00000380152.7:c.781G>C ENSP00000369497.3:p.Ala261Pro
ENST00000530893.6:n.979G>C
ENST00000544455.5:c.781G>C ENSP00000439902.1:p.Ala261Pro
ENST00000614259.1:n.781G>C
NM_000059.3:c.781G>C , LRG_293t1:c.781G>C NP_000050.2:p.Ala261Pro
XM_011535203.1:c.781G>C XP_011533505.1:p.Ala261Pro
XM_011535204.1:c.781G>C XP_011533506.1:p.Ala261Pro
XM_011535205.1:c.781G>C XP_011533507.1:p.Ala261Pro
NM_000059.4:c.781G>C MANE Select NP_000050.3:p.Ala261Pro