Canonical Allele Identifier: CA2082835821
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398411C= , CM000675.2:g.32398411C= GRCh38
NC_000013.10:g.32972548C= , CM000675.1:g.32972548C= GRCh37
NC_000013.9:g.31870548C= NCBI36
NG_012772.3:g.87932C= , LRG_293:g.87932C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*421C= ENSP00000434898.2:n.*421C=
ENST00000528762.2:c.*1265C= ENSP00000433168.2:n.*1265C=
ENST00000530893.7:c.9529C= ENSP00000499438.2:p.Pro3177=
ENST00000665585.2:c.*1460C= ENSP00000499570.2:n.*1460C=
ENST00000700202.2:c.9847C= ENSP00000514856.2:p.Pro3283=
ENST00000700202.1:c.2314C= ENSP00000514856.1:p.Pro772=
ENST00000700203.1:n.2025C=
ENST00000380152.8:c.9898C= MANE Select ENSP00000369497.3:p.Pro3300=
ENST00000544455.6:c.9898C= ENSP00000439902.1:p.Pro3300=
ENST00000614259.2:c.9906C= ENSP00000506251.1:n.9906C=
ENST00000680887.1:c.9898C= ENSP00000505508.1:p.Pro3300=
ENST00000380152.7:c.9898C= ENSP00000369497.3:p.Pro3300=
ENST00000533776.1:n.486C=
ENST00000544455.5:c.9898C= ENSP00000439902.1:p.Pro3300=
NM_000059.3:c.9898C= , LRG_293t1:c.9898C= NP_000050.2:p.Pro3300=
XM_011535203.1:c.9898C= XP_011533505.1:p.Pro3300=
XM_011535204.1:c.9802C= XP_011533506.1:p.Pro3268=
NM_000059.4:c.9898C= MANE Select NP_000050.3:p.Pro3300=