Canonical Allele Identifier: CA2082759304
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32330972_32330973delinsAT , CM000675.2:g.32330972_32330973delinsAT GRCh38
NC_000013.10:g.32905109_32905110delinsAT , CM000675.1:g.32905109_32905110delinsAT GRCh37
NC_000013.9:g.31803109_31803110delinsAT NCBI36
NG_012772.3:g.20493_20494delinsAT , LRG_293:g.20493_20494delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.735_736delinsAT ENSP00000434898.2:p.Arg245=
ENST00000528762.2:c.735_736delinsAT ENSP00000433168.2:p.Arg245=
ENST00000530893.7:c.366_367delinsAT ENSP00000499438.2:p.Arg122=
ENST00000665585.2:c.735_736delinsAT ENSP00000499570.2:p.Arg245=
ENST00000666593.2:c.735_736delinsAT ENSP00000499256.2:p.Arg245=
ENST00000700202.2:c.735_736delinsAT ENSP00000514856.2:p.Arg245=
ENST00000700201.1:c.*514_*515delinsAT ENSP00000514855.1:n.*514_*515delinsAT
ENST00000380152.8:c.735_736delinsAT MANE Select ENSP00000369497.3:p.Arg245=
ENST00000544455.6:c.735_736delinsAT ENSP00000439902.1:p.Arg245=
ENST00000614259.2:c.735_736delinsAT ENSP00000506251.1:p.Arg245=
ENST00000680887.1:c.735_736delinsAT ENSP00000505508.1:p.Arg245=
ENST00000380152.7:c.735_736delinsAT ENSP00000369497.3:p.Arg245=
ENST00000530893.6:n.933_934delinsAT
ENST00000544455.5:c.735_736delinsAT ENSP00000439902.1:p.Arg245=
ENST00000614259.1:n.735_736delinsAT
NM_000059.3:c.735_736delinsAT , LRG_293t1:c.735_736delinsAT NP_000050.2:p.Arg245=
XM_011535203.1:c.735_736delinsAT XP_011533505.1:p.Arg245=
XM_011535204.1:c.735_736delinsAT XP_011533506.1:p.Arg245=
XM_011535205.1:c.735_736delinsAT XP_011533507.1:p.Arg245=
NM_000059.4:c.735_736delinsAT MANE Select NP_000050.3:p.Arg245=