Canonical Allele Identifier: CA2082836277
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379464_32379465delinsAC , CM000675.2:g.32379464_32379465delinsAC GRCh38
NC_000013.10:g.32953601_32953602delinsAC , CM000675.1:g.32953601_32953602delinsAC GRCh37
NC_000013.9:g.31851601_31851602delinsAC NCBI36
NG_012772.3:g.68985_68986delinsAC , LRG_293:g.68985_68986delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8902_8903delinsAC ENSP00000434898.2:p.Thr2968=
ENST00000528762.2:c.*269_*270delinsAC ENSP00000433168.2:n.*269_*270delinsAC
ENST00000530893.7:c.8533_8534delinsAC ENSP00000499438.2:p.Thr2845=
ENST00000665585.2:c.*464_*465delinsAC ENSP00000499570.2:n.*464_*465delinsAC
ENST00000666593.2:c.8902_8903delinsAC ENSP00000499256.2:p.Thr2968=
ENST00000700202.2:c.8902_8903delinsAC ENSP00000514856.2:p.Thr2968=
ENST00000700202.1:c.1369_1370delinsAC ENSP00000514856.1:p.Thr457=
ENST00000700203.1:n.1029_1030delinsAC
ENST00000380152.8:c.8902_8903delinsAC MANE Select ENSP00000369497.3:p.Thr2968=
ENST00000544455.6:c.8902_8903delinsAC ENSP00000439902.1:p.Thr2968=
ENST00000614259.2:c.8910_8911delinsAC ENSP00000506251.1:n.8910_8911delinsAC
ENST00000665585.1:c.1780_1781delinsAC
ENST00000680887.1:c.8902_8903delinsAC ENSP00000505508.1:p.Thr2968=
ENST00000380152.7:c.8902_8903delinsAC ENSP00000369497.3:p.Thr2968=
ENST00000528762.1:c.464_465delinsAC ENSP00000433168.1:n.464_465delinsAC
ENST00000544455.5:c.8902_8903delinsAC ENSP00000439902.1:p.Thr2968=
NM_000059.3:c.8902_8903delinsAC , LRG_293t1:c.8902_8903delinsAC NP_000050.2:p.Thr2968=
XM_011535203.1:c.8902_8903delinsAC XP_011533505.1:p.Thr2968=
XM_011535204.1:c.8806_8807delinsAC XP_011533506.1:p.Thr2936=
XM_011535205.1:c.8755-286_8755-285delinsAC XP_011533507.1:n.8755-286_8755-285delinsAC
NM_000059.4:c.8902_8903delinsAC MANE Select NP_000050.3:p.Thr2968=