Canonical Allele Identifier: CA2082814351
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32370543_32370544delinsGC , CM000675.2:g.32370543_32370544delinsGC GRCh38
NC_000013.10:g.32944680_32944681delinsGC , CM000675.1:g.32944680_32944681delinsGC GRCh37
NC_000013.9:g.31842680_31842681delinsGC NCBI36
NG_012772.3:g.60064_60065delinsGC , LRG_293:g.60064_60065delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8473_8474delinsGC ENSP00000434898.2:p.Ala2825=
ENST00000528762.2:c.8473_8474delinsGC ENSP00000433168.2:p.Ala2825=
ENST00000530893.7:c.8104_8105delinsGC ENSP00000499438.2:p.Ala2702=
ENST00000665585.2:c.8473_8474delinsGC ENSP00000499570.2:p.Ala2825=
ENST00000666593.2:c.8473_8474delinsGC ENSP00000499256.2:p.Ala2825=
ENST00000700202.2:c.8473_8474delinsGC ENSP00000514856.2:p.Ala2825=
ENST00000700202.1:c.940_941delinsGC ENSP00000514856.1:p.Ala314=
ENST00000380152.8:c.8473_8474delinsGC MANE Select ENSP00000369497.3:p.Ala2825=
ENST00000544455.6:c.8473_8474delinsGC ENSP00000439902.1:p.Ala2825=
ENST00000614259.2:c.8481_8482delinsGC ENSP00000506251.1:n.8481_8482delinsGC
ENST00000665585.1:c.1038_1039delinsGC
ENST00000680887.1:c.8473_8474delinsGC ENSP00000505508.1:p.Ala2825=
ENST00000380152.7:c.8473_8474delinsGC ENSP00000369497.3:p.Ala2825=
ENST00000544455.5:c.8473_8474delinsGC ENSP00000439902.1:p.Ala2825=
NM_000059.3:c.8473_8474delinsGC , LRG_293t1:c.8473_8474delinsGC NP_000050.2:p.Ala2825=
XM_011535203.1:c.8473_8474delinsGC XP_011533505.1:p.Ala2825=
XM_011535204.1:c.8377_8378delinsGC XP_011533506.1:p.Ala2793=
XM_011535205.1:c.8473_8474delinsGC XP_011533507.1:p.Ala2825=
NM_000059.4:c.8473_8474delinsGC MANE Select NP_000050.3:p.Ala2825=