Canonical Allele Identifier: CA2082837332
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379742_32379746delinsCCAAA , CM000675.2:g.32379742_32379746delinsCCAAA GRCh38
NC_000013.10:g.32953879_32953883delinsCCAAA , CM000675.1:g.32953879_32953883delinsCCAAA GRCh37
NC_000013.9:g.31851879_31851883delinsCCAAA NCBI36
NG_012772.3:g.69263_69267delinsCCAAA , LRG_293:g.69263_69267delinsCCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8954-8_8954-4delinsCCAAA ENSP00000434898.2:n.8954-8_8954-4delinsCCAAA
ENST00000528762.2:c.*321-8_*321-4delinsCCAAA ENSP00000433168.2:n.*321-8_*321-4delinsCCAAA
ENST00000530893.7:c.8585-8_8585-4delinsCCAAA ENSP00000499438.2:n.8585-8_8585-4delinsCCAAA
ENST00000665585.2:c.*516-8_*516-4delinsCCAAA ENSP00000499570.2:n.*516-8_*516-4delinsCCAAA
ENST00000666593.2:c.8954-8_8954-4delinsCCAAA ENSP00000499256.2:n.8954-8_8954-4delinsCCAAA
ENST00000700202.2:c.8954-59_8954-55delinsCCAAA ENSP00000514856.2:n.8954-59_8954-55delinsCCAAA
ENST00000700202.1:c.1421-59_1421-55delinsCCAAA ENSP00000514856.1:n.1421-59_1421-55delinsCCAAA
ENST00000700203.1:n.1081-8_1081-4delinsCCAAA
ENST00000380152.8:c.8954-8_8954-4delinsCCAAA MANE Select ENSP00000369497.3:n.8954-8_8954-4delinsCCAAA
ENST00000544455.6:c.8954-8_8954-4delinsCCAAA ENSP00000439902.1:n.8954-8_8954-4delinsCCAAA
ENST00000614259.2:c.8962-8_8962-4delinsCCAAA ENSP00000506251.1:n.8962-8_8962-4delinsCCAAA
ENST00000665585.1:c.1832-8_1832-4delinsCCAAA
ENST00000680887.1:c.8954-8_8954-4delinsCCAAA ENSP00000505508.1:n.8954-8_8954-4delinsCCAAA
ENST00000380152.7:c.8954-8_8954-4delinsCCAAA ENSP00000369497.3:n.8954-8_8954-4delinsCCAAA
ENST00000544455.5:c.8954-8_8954-4delinsCCAAA ENSP00000439902.1:n.8954-8_8954-4delinsCCAAA
NM_000059.3:c.8954-8_8954-4delinsCCAAA , LRG_293t1:c.8954-8_8954-4delinsCCAAA NP_000050.2:n.8954-8_8954-4delinsCCAAA
XM_011535203.1:c.8954-8_8954-4delinsCCAAA XP_011533505.1:n.8954-8_8954-4delinsCCAAA
XM_011535204.1:c.8858-8_8858-4delinsCCAAA XP_011533506.1:n.8858-8_8858-4delinsCCAAA
XM_011535205.1:c.8755-8_8755-4delinsCCAAA XP_011533507.1:n.8755-8_8755-4delinsCCAAA
NM_000059.4:c.8954-8_8954-4delinsCCAAA MANE Select NP_000050.3:n.8954-8_8954-4delinsCCAAA