Canonical Allele Identifier: CA919242483
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1566224572

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32333364_32333365dup , CM000675.2:g.32333364_32333365dup GRCh38
NC_000013.10:g.32907501_32907502dup , CM000675.1:g.32907501_32907502dup GRCh37
NC_000013.9:g.31805501_31805502dup NCBI36
NG_012772.3:g.22885_22886dup , LRG_293:g.22885_22886dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1886_1887dup ENSP00000434898.2:p.Thr630LeufsTer15
ENST00000528762.2:c.1886_1887dup ENSP00000433168.2:p.Thr630LeufsTer15
ENST00000530893.7:c.1517_1518dup ENSP00000499438.2:p.Thr507LeufsTer15
ENST00000665585.2:c.1886_1887dup ENSP00000499570.2:p.Thr630LeufsTer15
ENST00000666593.2:c.1886_1887dup ENSP00000499256.2:p.Thr630LeufsTer15
ENST00000700202.2:c.1886_1887dup ENSP00000514856.2:p.Thr630LeufsTer15
ENST00000380152.8:c.1886_1887dup MANE Select ENSP00000369497.3:p.Thr630LeufsTer15
ENST00000544455.6:c.1886_1887dup ENSP00000439902.1:p.Thr630LeufsTer15
ENST00000614259.2:c.1886_1887dup ENSP00000506251.1:p.Thr630LeufsTer15
ENST00000680887.1:c.1886_1887dup ENSP00000505508.1:p.Thr630LeufsTer15
ENST00000380152.7:c.1886_1887dup ENSP00000369497.3:p.Thr630LeufsTer15
ENST00000544455.5:c.1886_1887dup ENSP00000439902.1:p.Thr630LeufsTer15
ENST00000614259.1:n.1886_1887dup
NM_000059.3:c.1886_1887dup , LRG_293t1:c.1886_1887dup NP_000050.2:p.Thr630LeufsTer15
XM_011535203.1:c.1886_1887dup XP_011533505.1:p.Thr630LeufsTer15
XM_011535204.1:c.1886_1887dup XP_011533506.1:p.Thr630LeufsTer15
XM_011535205.1:c.1886_1887dup XP_011533507.1:p.Thr630LeufsTer15
NM_000059.4:c.1886_1887dup MANE Select NP_000050.3:p.Thr630LeufsTer15