Canonical Allele Identifier: CA2082835542
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32398363A= , CM000675.2:g.32398363A= GRCh38
NC_000013.10:g.32972500A= , CM000675.1:g.32972500A= GRCh37
NC_000013.9:g.31870500A= NCBI36
NG_012772.3:g.87884A= , LRG_293:g.87884A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*373A= ENSP00000434898.2:n.*373A=
ENST00000528762.2:c.*1217A= ENSP00000433168.2:n.*1217A=
ENST00000530893.7:c.9481A= ENSP00000499438.2:p.Ser3161=
ENST00000665585.2:c.*1412A= ENSP00000499570.2:n.*1412A=
ENST00000700202.2:c.9799A= ENSP00000514856.2:p.Ser3267=
ENST00000700202.1:c.2266A= ENSP00000514856.1:p.Ser756=
ENST00000700203.1:n.1977A=
ENST00000380152.8:c.9850A= MANE Select ENSP00000369497.3:p.Ser3284=
ENST00000544455.6:c.9850A= ENSP00000439902.1:p.Ser3284=
ENST00000614259.2:c.9858A= ENSP00000506251.1:n.9858A=
ENST00000680887.1:c.9850A= ENSP00000505508.1:p.Ser3284=
ENST00000380152.7:c.9850A= ENSP00000369497.3:p.Ser3284=
ENST00000533776.1:n.438A=
ENST00000544455.5:c.9850A= ENSP00000439902.1:p.Ser3284=
NM_000059.3:c.9850A= , LRG_293t1:c.9850A= NP_000050.2:p.Ser3284=
XM_011535203.1:c.9850A= XP_011533505.1:p.Ser3284=
XM_011535204.1:c.9754A= XP_011533506.1:p.Ser3252=
NM_000059.4:c.9850A= MANE Select NP_000050.3:p.Ser3284=