Canonical Allele Identifier: CA2082756136
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32329262_32329267delinsATAGTT , CM000675.2:g.32329262_32329267delinsATAGTT GRCh38
NC_000013.10:g.32903399_32903404delinsATAGTT , CM000675.1:g.32903399_32903404delinsATAGTT GRCh37
NC_000013.9:g.31801399_31801404delinsATAGTT NCBI36
NG_012772.3:g.18783_18788delinsATAGTT , LRG_293:g.18783_18788delinsATAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.632-181_632-176delinsATAGTT ENSP00000434898.2:n.632-181_632-176delinsATAGTT
ENST00000528762.2:c.632-181_632-176delinsATAGTT ENSP00000433168.2:n.632-181_632-176delinsATAGTT
ENST00000530893.7:c.263-181_263-176delinsATAGTT ENSP00000499438.2:n.263-181_263-176delinsATAGTT
ENST00000665585.2:c.632-181_632-176delinsATAGTT ENSP00000499570.2:n.632-181_632-176delinsATAGTT
ENST00000666593.2:c.632-181_632-176delinsATAGTT ENSP00000499256.2:n.632-181_632-176delinsATAGTT
ENST00000700202.2:c.632-181_632-176delinsATAGTT ENSP00000514856.2:n.632-181_632-176delinsATAGTT
ENST00000700201.1:c.*411-181_*411-176delinsATAGTT ENSP00000514855.1:n.*411-181_*411-176delinsATAGTT
ENST00000380152.8:c.632-181_632-176delinsATAGTT MANE Select ENSP00000369497.3:n.632-181_632-176delinsATAGTT
ENST00000544455.6:c.632-181_632-176delinsATAGTT ENSP00000439902.1:n.632-181_632-176delinsATAGTT
ENST00000614259.2:c.632-181_632-176delinsATAGTT ENSP00000506251.1:n.632-181_632-176delinsATAGTT
ENST00000680887.1:c.632-181_632-176delinsATAGTT ENSP00000505508.1:n.632-181_632-176delinsATAGTT
ENST00000380152.7:c.632-181_632-176delinsATAGTT ENSP00000369497.3:n.632-181_632-176delinsATAGTT
ENST00000530893.6:n.830-181_830-176delinsATAGTT
ENST00000544455.5:c.632-181_632-176delinsATAGTT ENSP00000439902.1:n.632-181_632-176delinsATAGTT
ENST00000614259.1:n.632-181_632-176delinsATAGTT
NM_000059.3:c.632-181_632-176delinsATAGTT , LRG_293t1:c.632-181_632-176delinsATAGTT NP_000050.2:n.632-181_632-176delinsATAGTT
XM_011535203.1:c.632-181_632-176delinsATAGTT XP_011533505.1:n.632-181_632-176delinsATAGTT
XM_011535204.1:c.632-181_632-176delinsATAGTT XP_011533506.1:n.632-181_632-176delinsATAGTT
XM_011535205.1:c.632-181_632-176delinsATAGTT XP_011533507.1:n.632-181_632-176delinsATAGTT
NM_000059.4:c.632-181_632-176delinsATAGTT MANE Select NP_000050.3:n.632-181_632-176delinsATAGTT