Canonical Allele Identifier: CA387766457
Gene: BRCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398360G>C , CM000675.2:g.32398360G>C GRCh38
NC_000013.10:g.32972497G>C , CM000675.1:g.32972497G>C GRCh37
NC_000013.9:g.31870497G>C NCBI36
NG_012772.3:g.87881G>C , LRG_293:g.87881G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*370G>C ENSP00000434898.2:n.*370G>C
ENST00000528762.2:c.*1214G>C ENSP00000433168.2:n.*1214G>C
ENST00000530893.7:c.9478G>C ENSP00000499438.2:p.Val3160Leu
ENST00000665585.2:c.*1409G>C ENSP00000499570.2:n.*1409G>C
ENST00000700202.2:c.9796G>C ENSP00000514856.2:p.Val3266Leu
ENST00000700202.1:c.2263G>C ENSP00000514856.1:p.Val755Leu
ENST00000700203.1:n.1974G>C
ENST00000380152.8:c.9847G>C MANE Select ENSP00000369497.3:p.Val3283Leu
ENST00000544455.6:c.9847G>C ENSP00000439902.1:p.Val3283Leu
ENST00000614259.2:c.9855G>C ENSP00000506251.1:n.9855G>C
ENST00000680887.1:c.9847G>C ENSP00000505508.1:p.Val3283Leu
ENST00000380152.7:c.9847G>C ENSP00000369497.3:p.Val3283Leu
ENST00000533776.1:n.435G>C
ENST00000544455.5:c.9847G>C ENSP00000439902.1:p.Val3283Leu
NM_000059.3:c.9847G>C , LRG_293t1:c.9847G>C NP_000050.2:p.Val3283Leu
XM_011535203.1:c.9847G>C XP_011533505.1:p.Val3283Leu
XM_011535204.1:c.9751G>C XP_011533506.1:p.Val3251Leu
NM_000059.4:c.9847G>C MANE Select NP_000050.3:p.Val3283Leu