Canonical Allele Identifier: CA2082769746
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32333089_32333091delinsAAG , CM000675.2:g.32333089_32333091delinsAAG GRCh38
NC_000013.10:g.32907226_32907228delinsAAG , CM000675.1:g.32907226_32907228delinsAAG GRCh37
NC_000013.9:g.31805226_31805228delinsAAG NCBI36
NG_012772.3:g.22610_22612delinsAAG , LRG_293:g.22610_22612delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1611_1613delinsAAG ENSP00000434898.2:p.Glu537=
ENST00000528762.2:c.1611_1613delinsAAG ENSP00000433168.2:p.Glu537=
ENST00000530893.7:c.1242_1244delinsAAG ENSP00000499438.2:p.Glu414=
ENST00000665585.2:c.1611_1613delinsAAG ENSP00000499570.2:p.Glu537=
ENST00000666593.2:c.1611_1613delinsAAG ENSP00000499256.2:p.Glu537=
ENST00000700202.2:c.1611_1613delinsAAG ENSP00000514856.2:p.Glu537=
ENST00000700201.1:c.*1390_*1392delinsAAG ENSP00000514855.1:n.*1390_*1392delinsAAG
ENST00000380152.8:c.1611_1613delinsAAG MANE Select ENSP00000369497.3:p.Glu537=
ENST00000544455.6:c.1611_1613delinsAAG ENSP00000439902.1:p.Glu537=
ENST00000614259.2:c.1611_1613delinsAAG ENSP00000506251.1:p.Glu537=
ENST00000680887.1:c.1611_1613delinsAAG ENSP00000505508.1:p.Glu537=
ENST00000380152.7:c.1611_1613delinsAAG ENSP00000369497.3:p.Glu537=
ENST00000530893.6:n.1809_1811delinsAAG
ENST00000544455.5:c.1611_1613delinsAAG ENSP00000439902.1:p.Glu537=
ENST00000614259.1:n.1611_1613delinsAAG
NM_000059.3:c.1611_1613delinsAAG , LRG_293t1:c.1611_1613delinsAAG NP_000050.2:p.Glu537=
XM_011535203.1:c.1611_1613delinsAAG XP_011533505.1:p.Glu537=
XM_011535204.1:c.1611_1613delinsAAG XP_011533506.1:p.Glu537=
XM_011535205.1:c.1611_1613delinsAAG XP_011533507.1:p.Glu537=
NM_000059.4:c.1611_1613delinsAAG MANE Select NP_000050.3:p.Glu537=