Canonical Allele Identifier: CA2082830426
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32396963C= , CM000675.2:g.32396963C= GRCh38
NC_000013.10:g.32971100C= , CM000675.1:g.32971100C= GRCh37
NC_000013.9:g.31869100C= NCBI36
NG_012772.3:g.86484C= , LRG_293:g.86484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*90C= ENSP00000434898.2:n.*90C=
ENST00000528762.2:c.*934C= ENSP00000433168.2:n.*934C=
ENST00000530893.7:c.9198C= ENSP00000499438.2:p.Pro3066=
ENST00000665585.2:c.*1129C= ENSP00000499570.2:n.*1129C=
ENST00000700202.2:c.9516C= ENSP00000514856.2:p.Pro3172=
ENST00000700202.1:c.1983C= ENSP00000514856.1:p.Pro661=
ENST00000700203.1:n.1694C=
ENST00000380152.8:c.9567C= MANE Select ENSP00000369497.3:p.Pro3189=
ENST00000544455.6:c.9567C= ENSP00000439902.1:p.Pro3189=
ENST00000614259.2:c.9575C= ENSP00000506251.1:n.9575C=
ENST00000665585.1:c.2445C=
ENST00000680887.1:c.9567C= ENSP00000505508.1:p.Pro3189=
ENST00000380152.7:c.9567C= ENSP00000369497.3:p.Pro3189=
ENST00000470094.1:c.650C=
ENST00000533776.1:n.155C=
ENST00000544455.5:c.9567C= ENSP00000439902.1:p.Pro3189=
NM_000059.3:c.9567C= , LRG_293t1:c.9567C= NP_000050.2:p.Pro3189=
XM_011535203.1:c.9567C= XP_011533505.1:p.Pro3189=
XM_011535204.1:c.9471C= XP_011533506.1:p.Pro3157=
NM_000059.4:c.9567C= MANE Select NP_000050.3:p.Pro3189=