Canonical Allele Identifier: CA2622602725
Gene: BRCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398112_32398127del , CM000675.2:g.32398112_32398127del GRCh38
NC_000013.10:g.32972249_32972264del , CM000675.1:g.32972249_32972264del GRCh37
NC_000013.9:g.31870249_31870264del NCBI36
NG_012772.3:g.87633_87648del , LRG_293:g.87633_87648del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*172-50_*172-35del ENSP00000434898.2:n.*172-50_*172-35del
ENST00000528762.2:c.*1016-50_*1016-35del ENSP00000433168.2:n.*1016-50_*1016-35del
ENST00000530893.7:c.9280-50_9280-35del ENSP00000499438.2:n.9280-50_9280-35del
ENST00000665585.2:c.*1211-50_*1211-35del ENSP00000499570.2:n.*1211-50_*1211-35del
ENST00000700202.2:c.9598-50_9598-35del ENSP00000514856.2:n.9598-50_9598-35del
ENST00000700202.1:c.2065-50_2065-35del ENSP00000514856.1:n.2065-50_2065-35del
ENST00000700203.1:n.1776-50_1776-35del
ENST00000380152.8:c.9649-50_9649-35del MANE Select ENSP00000369497.3:n.9649-50_9649-35del
ENST00000544455.6:c.9649-50_9649-35del ENSP00000439902.1:n.9649-50_9649-35del
ENST00000614259.2:c.9657-50_9657-35del ENSP00000506251.1:n.9657-50_9657-35del
ENST00000665585.1:c.2527-50_2527-35del
ENST00000680887.1:c.9649-50_9649-35del ENSP00000505508.1:n.9649-50_9649-35del
ENST00000380152.7:c.9649-50_9649-35del ENSP00000369497.3:n.9649-50_9649-35del
ENST00000470094.1:c.732-50_732-35del
ENST00000533776.1:n.237-50_237-35del
ENST00000544455.5:c.9649-50_9649-35del ENSP00000439902.1:n.9649-50_9649-35del
NM_000059.3:c.9649-50_9649-35del , LRG_293t1:c.9649-50_9649-35del NP_000050.2:n.9649-50_9649-35del
XM_011535203.1:c.9649-50_9649-35del XP_011533505.1:n.9649-50_9649-35del
XM_011535204.1:c.9553-50_9553-35del XP_011533506.1:n.9553-50_9553-35del
NM_000059.4:c.9649-50_9649-35del MANE Select NP_000050.3:n.9649-50_9649-35del