Canonical Allele Identifier: CA2082821872
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394694G= , CM000675.2:g.32394694G= GRCh38
NC_000013.10:g.32968831G= , CM000675.1:g.32968831G= GRCh37
NC_000013.9:g.31866831G= NCBI36
NG_012772.3:g.84215G= , LRG_293:g.84215G=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.9262G= ENSP00000434898.2:p.Ala3088=
ENST00000528762.2:c.*629G= ENSP00000433168.2:n.*629G=
ENST00000530893.7:c.8893G= ENSP00000499438.2:p.Ala2965=
ENST00000665585.2:c.*824G= ENSP00000499570.2:n.*824G=
ENST00000666593.2:c.*107G= ENSP00000499256.2:n.*107G=
ENST00000700202.2:c.9211G= ENSP00000514856.2:p.Ala3071=
ENST00000700202.1:c.1678G= ENSP00000514856.1:p.Ala560=
ENST00000700203.1:n.1389G=
ENST00000380152.8:c.9262G= MANE Select ENSP00000369497.3:p.Ala3088=
ENST00000544455.6:c.9262G= ENSP00000439902.1:p.Ala3088=
ENST00000614259.2:c.9270G= ENSP00000506251.1:n.9270G=
ENST00000665585.1:c.2140G=
ENST00000666593.1:c.284G= ENSP00000499256.1:n.284G=
ENST00000680887.1:c.9262G= ENSP00000505508.1:p.Ala3088=
ENST00000380152.7:c.9262G= ENSP00000369497.3:p.Ala3088=
ENST00000470094.1:c.219G=
ENST00000544455.5:c.9262G= ENSP00000439902.1:p.Ala3088=
NM_000059.3:c.9262G= , LRG_293t1:c.9262G= NP_000050.2:p.Ala3088=
XM_011535203.1:c.9262G= XP_011533505.1:p.Ala3088=
XM_011535204.1:c.9166G= XP_011533506.1:p.Ala3056=
NM_000059.4:c.9262G= MANE Select NP_000050.3:p.Ala3088=