Canonical Allele Identifier: CA2082833901
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398170T= , CM000675.2:g.32398170T= GRCh38
NC_000013.10:g.32972307T= , CM000675.1:g.32972307T= GRCh37
NC_000013.9:g.31870307T= NCBI36
NG_012772.3:g.87691T= , LRG_293:g.87691T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*180T= ENSP00000434898.2:n.*180T=
ENST00000528762.2:c.*1024T= ENSP00000433168.2:n.*1024T=
ENST00000530893.7:c.9288T= ENSP00000499438.2:p.Ser3096=
ENST00000665585.2:c.*1219T= ENSP00000499570.2:n.*1219T=
ENST00000700202.2:c.9606T= ENSP00000514856.2:p.Ser3202=
ENST00000700202.1:c.2073T= ENSP00000514856.1:p.Ser691=
ENST00000700203.1:n.1784T=
ENST00000380152.8:c.9657T= MANE Select ENSP00000369497.3:p.Ser3219=
ENST00000544455.6:c.9657T= ENSP00000439902.1:p.Ser3219=
ENST00000614259.2:c.9665T= ENSP00000506251.1:n.9665T=
ENST00000665585.1:c.2535T=
ENST00000680887.1:c.9657T= ENSP00000505508.1:p.Ser3219=
ENST00000380152.7:c.9657T= ENSP00000369497.3:p.Ser3219=
ENST00000470094.1:c.740T=
ENST00000533776.1:n.245T=
ENST00000544455.5:c.9657T= ENSP00000439902.1:p.Ser3219=
NM_000059.3:c.9657T= , LRG_293t1:c.9657T= NP_000050.2:p.Ser3219=
XM_011535203.1:c.9657T= XP_011533505.1:p.Ser3219=
XM_011535204.1:c.9561T= XP_011533506.1:p.Ser3187=
NM_000059.4:c.9657T= MANE Select NP_000050.3:p.Ser3219=