Canonical Allele Identifier: CA2082838009
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398696_32398697delinsGA , CM000675.2:g.32398696_32398697delinsGA GRCh38
NC_000013.10:g.32972833_32972834delinsGA , CM000675.1:g.32972833_32972834delinsGA GRCh37
NC_000013.9:g.31870833_31870834delinsGA NCBI36
NG_012772.3:g.88217_88218delinsGA , LRG_293:g.88217_88218delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*706_*707delinsGA ENSP00000434898.2:n.*706_*707delinsGA
ENST00000528762.2:c.*1550_*1551delinsGA ENSP00000433168.2:n.*1550_*1551delinsGA
ENST00000530893.7:c.9814_9815delinsGA ENSP00000499438.2:p.Glu3272=
ENST00000665585.2:c.*1745_*1746delinsGA ENSP00000499570.2:n.*1745_*1746delinsGA
ENST00000700202.2:c.10132_10133delinsGA ENSP00000514856.2:p.Glu3378=
ENST00000700202.1:c.2599_2600delinsGA ENSP00000514856.1:p.Glu867=
ENST00000700203.1:n.2310_2311delinsGA
ENST00000380152.8:c.10183_10184delinsGA MANE Select ENSP00000369497.3:p.Glu3395=
ENST00000544455.6:c.10183_10184delinsGA ENSP00000439902.1:p.Glu3395=
ENST00000614259.2:c.10191_10192delinsGA ENSP00000506251.1:n.10191_10192delinsGA
ENST00000680887.1:c.10183_10184delinsGA ENSP00000505508.1:p.Glu3395=
ENST00000380152.7:c.10183_10184delinsGA ENSP00000369497.3:p.Glu3395=
ENST00000544455.5:c.10183_10184delinsGA ENSP00000439902.1:p.Glu3395=
NM_000059.3:c.10183_10184delinsGA , LRG_293t1:c.10183_10184delinsGA NP_000050.2:p.Glu3395=
XM_011535203.1:c.10183_10184delinsGA XP_011533505.1:p.Glu3395=
XM_011535204.1:c.10087_10088delinsGA XP_011533506.1:p.Glu3363=
NM_000059.4:c.10183_10184delinsGA MANE Select NP_000050.3:p.Glu3395=