Canonical Allele Identifier: CA2082818011
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32357794_32357795delinsCA , CM000675.2:g.32357794_32357795delinsCA GRCh38
NC_000013.10:g.32931931_32931932delinsCA , CM000675.1:g.32931931_32931932delinsCA GRCh37
NC_000013.9:g.31829931_31829932delinsCA NCBI36
NG_012772.3:g.47315_47316delinsCA , LRG_293:g.47315_47316delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7670_7671delinsCA ENSP00000434898.2:p.Ala2557=
ENST00000528762.2:c.7670_7671delinsCA ENSP00000433168.2:p.Ala2557=
ENST00000530893.7:c.7301_7302delinsCA ENSP00000499438.2:p.Ala2434=
ENST00000665585.2:c.7670_7671delinsCA ENSP00000499570.2:p.Ala2557=
ENST00000666593.2:c.7670_7671delinsCA ENSP00000499256.2:p.Ala2557=
ENST00000700202.2:c.7670_7671delinsCA ENSP00000514856.2:p.Ala2557=
ENST00000700202.1:c.137_138delinsCA ENSP00000514856.1:p.Ala46=
ENST00000380152.8:c.7670_7671delinsCA MANE Select ENSP00000369497.3:p.Ala2557=
ENST00000544455.6:c.7670_7671delinsCA ENSP00000439902.1:p.Ala2557=
ENST00000614259.2:c.7670_7671delinsCA ENSP00000506251.1:p.Ala2557=
ENST00000665585.1:c.235_236delinsCA
ENST00000680887.1:c.7670_7671delinsCA ENSP00000505508.1:p.Ala2557=
ENST00000380152.7:c.7670_7671delinsCA ENSP00000369497.3:p.Ala2557=
ENST00000544455.5:c.7670_7671delinsCA ENSP00000439902.1:p.Ala2557=
ENST00000614259.1:n.7670_7671delinsCA
NM_000059.3:c.7670_7671delinsCA , LRG_293t1:c.7670_7671delinsCA NP_000050.2:p.Ala2557=
XM_011535203.1:c.7670_7671delinsCA XP_011533505.1:p.Ala2557=
XM_011535204.1:c.7574_7575delinsCA XP_011533506.1:p.Ala2525=
XM_011535205.1:c.7670_7671delinsCA XP_011533507.1:p.Ala2557=
NM_000059.4:c.7670_7671delinsCA MANE Select NP_000050.3:p.Ala2557=