Canonical Allele Identifier: CA2082750108
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32326138_32326143delinsAGAGAT , CM000675.2:g.32326138_32326143delinsAGAGAT GRCh38
NC_000013.10:g.32900275_32900280delinsAGAGAT , CM000675.1:g.32900275_32900280delinsAGAGAT GRCh37
NC_000013.9:g.31798275_31798280delinsAGAGAT NCBI36
NG_012772.3:g.15659_15664delinsAGAGAT , LRG_293:g.15659_15664delinsAGAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.463_468delinsAGAGAT ENSP00000434898.2:p.Arg155=
ENST00000528762.2:c.463_468delinsAGAGAT ENSP00000433168.2:p.Arg155=
ENST00000530893.7:c.94_99delinsAGAGAT ENSP00000499438.2:p.Arg32=
ENST00000665585.2:c.463_468delinsAGAGAT ENSP00000499570.2:p.Arg155=
ENST00000666593.2:c.463_468delinsAGAGAT ENSP00000499256.2:p.Arg155=
ENST00000700202.2:c.463_468delinsAGAGAT ENSP00000514856.2:p.Arg155=
ENST00000700200.1:n.334_339delinsAGAGAT
ENST00000700201.1:c.*242_*247delinsAGAGAT ENSP00000514855.1:n.*242_*247delinsAGAGAT
ENST00000380152.8:c.463_468delinsAGAGAT MANE Select ENSP00000369497.3:p.Arg155=
ENST00000544455.6:c.463_468delinsAGAGAT ENSP00000439902.1:p.Arg155=
ENST00000614259.2:c.463_468delinsAGAGAT ENSP00000506251.1:p.Arg155=
ENST00000680887.1:c.463_468delinsAGAGAT ENSP00000505508.1:p.Arg155=
ENST00000380152.7:c.463_468delinsAGAGAT ENSP00000369497.3:p.Arg155=
ENST00000530893.6:n.661_666delinsAGAGAT
ENST00000544455.5:c.463_468delinsAGAGAT ENSP00000439902.1:p.Arg155=
ENST00000614259.1:n.463_468delinsAGAGAT
NM_000059.3:c.463_468delinsAGAGAT , LRG_293t1:c.463_468delinsAGAGAT NP_000050.2:p.Arg155=
XM_011535203.1:c.463_468delinsAGAGAT XP_011533505.1:p.Arg155=
XM_011535204.1:c.463_468delinsAGAGAT XP_011533506.1:p.Arg155=
XM_011535205.1:c.463_468delinsAGAGAT XP_011533507.1:p.Arg155=
NM_000059.4:c.463_468delinsAGAGAT MANE Select NP_000050.3:p.Arg155=