Canonical Allele Identifier: CA2082835497
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398353_32398354delinsTC , CM000675.2:g.32398353_32398354delinsTC GRCh38
NC_000013.10:g.32972490_32972491delinsTC , CM000675.1:g.32972490_32972491delinsTC GRCh37
NC_000013.9:g.31870490_31870491delinsTC NCBI36
NG_012772.3:g.87874_87875delinsTC , LRG_293:g.87874_87875delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*363_*364delinsTC ENSP00000434898.2:n.*363_*364delinsTC
ENST00000528762.2:c.*1207_*1208delinsTC ENSP00000433168.2:n.*1207_*1208delinsTC
ENST00000530893.7:c.9471_9472delinsTC ENSP00000499438.2:p.Pro3157=
ENST00000665585.2:c.*1402_*1403delinsTC ENSP00000499570.2:n.*1402_*1403delinsTC
ENST00000700202.2:c.9789_9790delinsTC ENSP00000514856.2:p.Pro3263=
ENST00000700202.1:c.2256_2257delinsTC ENSP00000514856.1:p.Pro752=
ENST00000700203.1:n.1967_1968delinsTC
ENST00000380152.8:c.9840_9841delinsTC MANE Select ENSP00000369497.3:p.Pro3280=
ENST00000544455.6:c.9840_9841delinsTC ENSP00000439902.1:p.Pro3280=
ENST00000614259.2:c.9848_9849delinsTC ENSP00000506251.1:n.9848_9849delinsTC
ENST00000680887.1:c.9840_9841delinsTC ENSP00000505508.1:p.Pro3280=
ENST00000380152.7:c.9840_9841delinsTC ENSP00000369497.3:p.Pro3280=
ENST00000533776.1:n.428_429delinsTC
ENST00000544455.5:c.9840_9841delinsTC ENSP00000439902.1:p.Pro3280=
NM_000059.3:c.9840_9841delinsTC , LRG_293t1:c.9840_9841delinsTC NP_000050.2:p.Pro3280=
XM_011535203.1:c.9840_9841delinsTC XP_011533505.1:p.Pro3280=
XM_011535204.1:c.9744_9745delinsTC XP_011533506.1:p.Pro3248=
NM_000059.4:c.9840_9841delinsTC MANE Select NP_000050.3:p.Pro3280=