Canonical Allele Identifier: CA2580602582
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398875A>G , CM000675.2:g.32398875A>G GRCh38
NC_000013.10:g.32973012A>G , CM000675.1:g.32973012A>G GRCh37
NC_000013.9:g.31871012A>G NCBI36
NG_012772.3:g.88396A>G , LRG_293:g.88396A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.*885A>G ENSP00000434898.2:n.*885A>G
ENST00000528762.2:c.*1729A>G ENSP00000433168.2:n.*1729A>G
ENST00000530893.7:c.*105A>G ENSP00000499438.2:n.*105A>G
ENST00000665585.2:c.*1924A>G ENSP00000499570.2:n.*1924A>G
ENST00000700202.2:c.*105A>G ENSP00000514856.2:n.*105A>G
ENST00000700203.1:n.2489A>G
ENST00000380152.8:c.*105A>G MANE Select ENSP00000369497.3:n.*105A>G
ENST00000544455.6:c.*105A>G ENSP00000439902.1:n.*105A>G
ENST00000614259.2:c.10370A>G ENSP00000506251.1:n.10370A>G
ENST00000680887.1:c.*105A>G ENSP00000505508.1:n.*105A>G
ENST00000380152.7:c.*105A>G ENSP00000369497.3:n.*105A>G
ENST00000544455.5:c.*105A>G ENSP00000439902.1:n.*105A>G
NM_000059.3:c.*105A>G , LRG_293t1:c.*105A>G NP_000050.2:n.*105A>G
XM_011535203.1:c.*105A>G XP_011533505.1:n.*105A>G
XM_011535204.1:c.*105A>G XP_011533506.1:n.*105A>G
NM_000059.4:c.*105A>G MANE Select NP_000050.3:n.*105A>G