Canonical Allele Identifier: CA2082837342
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379744A= , CM000675.2:g.32379744A= GRCh38
NC_000013.10:g.32953881A= , CM000675.1:g.32953881A= GRCh37
NC_000013.9:g.31851881A= NCBI36
NG_012772.3:g.69265A= , LRG_293:g.69265A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8954-6A= ENSP00000434898.2:n.8954-6A=
ENST00000528762.2:c.*321-6A= ENSP00000433168.2:n.*321-6A=
ENST00000530893.7:c.8585-6A= ENSP00000499438.2:n.8585-6A=
ENST00000665585.2:c.*516-6A= ENSP00000499570.2:n.*516-6A=
ENST00000666593.2:c.8954-6A= ENSP00000499256.2:n.8954-6A=
ENST00000700202.2:c.8954-57A= ENSP00000514856.2:n.8954-57A=
ENST00000700202.1:c.1421-57A= ENSP00000514856.1:n.1421-57A=
ENST00000700203.1:n.1081-6A=
ENST00000380152.8:c.8954-6A= MANE Select ENSP00000369497.3:n.8954-6A=
ENST00000544455.6:c.8954-6A= ENSP00000439902.1:n.8954-6A=
ENST00000614259.2:c.8962-6A= ENSP00000506251.1:n.8962-6A=
ENST00000665585.1:c.1832-6A=
ENST00000680887.1:c.8954-6A= ENSP00000505508.1:n.8954-6A=
ENST00000380152.7:c.8954-6A= ENSP00000369497.3:n.8954-6A=
ENST00000544455.5:c.8954-6A= ENSP00000439902.1:n.8954-6A=
NM_000059.3:c.8954-6A= , LRG_293t1:c.8954-6A= NP_000050.2:n.8954-6A=
XM_011535203.1:c.8954-6A= XP_011533505.1:n.8954-6A=
XM_011535204.1:c.8858-6A= XP_011533506.1:n.8858-6A=
XM_011535205.1:c.8755-6A= XP_011533507.1:n.8755-6A=
NM_000059.4:c.8954-6A= MANE Select NP_000050.3:n.8954-6A=