Canonical Allele Identifier: CA2082836573
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379491_32379492delinsTA , CM000675.2:g.32379491_32379492delinsTA GRCh38
NC_000013.10:g.32953628_32953629delinsTA , CM000675.1:g.32953628_32953629delinsTA GRCh37
NC_000013.9:g.31851628_31851629delinsTA NCBI36
NG_012772.3:g.69012_69013delinsTA , LRG_293:g.69012_69013delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8929_8930delinsTA ENSP00000434898.2:p.Tyr2977=
ENST00000528762.2:c.*296_*297delinsTA ENSP00000433168.2:n.*296_*297delinsTA
ENST00000530893.7:c.8560_8561delinsTA ENSP00000499438.2:p.Tyr2854=
ENST00000665585.2:c.*491_*492delinsTA ENSP00000499570.2:n.*491_*492delinsTA
ENST00000666593.2:c.8929_8930delinsTA ENSP00000499256.2:p.Tyr2977=
ENST00000700202.2:c.8929_8930delinsTA ENSP00000514856.2:p.Tyr2977=
ENST00000700202.1:c.1396_1397delinsTA ENSP00000514856.1:p.Tyr466=
ENST00000700203.1:n.1056_1057delinsTA
ENST00000380152.8:c.8929_8930delinsTA MANE Select ENSP00000369497.3:p.Tyr2977=
ENST00000544455.6:c.8929_8930delinsTA ENSP00000439902.1:p.Tyr2977=
ENST00000614259.2:c.8937_8938delinsTA ENSP00000506251.1:n.8937_8938delinsTA
ENST00000665585.1:c.1807_1808delinsTA
ENST00000680887.1:c.8929_8930delinsTA ENSP00000505508.1:p.Tyr2977=
ENST00000380152.7:c.8929_8930delinsTA ENSP00000369497.3:p.Tyr2977=
ENST00000528762.1:c.491_492delinsTA ENSP00000433168.1:n.491_492delinsTA
ENST00000544455.5:c.8929_8930delinsTA ENSP00000439902.1:p.Tyr2977=
NM_000059.3:c.8929_8930delinsTA , LRG_293t1:c.8929_8930delinsTA NP_000050.2:p.Tyr2977=
XM_011535203.1:c.8929_8930delinsTA XP_011533505.1:p.Tyr2977=
XM_011535204.1:c.8833_8834delinsTA XP_011533506.1:p.Tyr2945=
XM_011535205.1:c.8755-259_8755-258delinsTA XP_011533507.1:n.8755-259_8755-258delinsTA
NM_000059.4:c.8929_8930delinsTA MANE Select NP_000050.3:p.Tyr2977=