Canonical Allele Identifier: CA2082828053
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32376672_32376674delinsAAC , CM000675.2:g.32376672_32376674delinsAAC GRCh38
NC_000013.10:g.32950809_32950811delinsAAC , CM000675.1:g.32950809_32950811delinsAAC GRCh37
NC_000013.9:g.31848809_31848811delinsAAC NCBI36
NG_012772.3:g.66193_66195delinsAAC , LRG_293:g.66193_66195delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8635_8637delinsAAC ENSP00000434898.2:p.Asn2879=
ENST00000528762.2:c.*2_*4delinsAAC ENSP00000433168.2:n.*2_*4delinsAAC
ENST00000530893.7:c.8266_8268delinsAAC ENSP00000499438.2:p.Asn2756=
ENST00000665585.2:c.*197_*199delinsAAC ENSP00000499570.2:n.*197_*199delinsAAC
ENST00000666593.2:c.8635_8637delinsAAC ENSP00000499256.2:p.Asn2879=
ENST00000700202.2:c.8635_8637delinsAAC ENSP00000514856.2:p.Asn2879=
ENST00000700202.1:c.1102_1104delinsAAC ENSP00000514856.1:p.Asn368=
ENST00000700203.1:n.762_764delinsAAC
ENST00000380152.8:c.8635_8637delinsAAC MANE Select ENSP00000369497.3:p.Asn2879=
ENST00000544455.6:c.8635_8637delinsAAC ENSP00000439902.1:p.Asn2879=
ENST00000614259.2:c.8643_8645delinsAAC ENSP00000506251.1:n.8643_8645delinsAAC
ENST00000665585.1:c.1513_1515delinsAAC
ENST00000680887.1:c.8635_8637delinsAAC ENSP00000505508.1:p.Asn2879=
ENST00000380152.7:c.8635_8637delinsAAC ENSP00000369497.3:p.Asn2879=
ENST00000528762.1:c.197_199delinsAAC ENSP00000433168.1:n.197_199delinsAAC
ENST00000544455.5:c.8635_8637delinsAAC ENSP00000439902.1:p.Asn2879=
NM_000059.3:c.8635_8637delinsAAC , LRG_293t1:c.8635_8637delinsAAC NP_000050.2:p.Asn2879=
XM_011535203.1:c.8635_8637delinsAAC XP_011533505.1:p.Asn2879=
XM_011535204.1:c.8539_8541delinsAAC XP_011533506.1:p.Asn2847=
XM_011535205.1:c.8635_8637delinsAAC XP_011533507.1:p.Asn2879=
NM_000059.4:c.8635_8637delinsAAC MANE Select NP_000050.3:p.Asn2879=