Canonical Allele Identifier: CA2082835315
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32363303T= , CM000675.2:g.32363303T= GRCh38
NC_000013.10:g.32937440T= , CM000675.1:g.32937440T= GRCh37
NC_000013.9:g.31835440T= NCBI36
NG_012772.3:g.52824T= , LRG_293:g.52824T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8101T= ENSP00000434898.2:p.Ser2701=
ENST00000528762.2:c.8101T= ENSP00000433168.2:p.Ser2701=
ENST00000530893.7:c.7732T= ENSP00000499438.2:p.Ser2578=
ENST00000665585.2:c.8101T= ENSP00000499570.2:p.Ser2701=
ENST00000666593.2:c.8101T= ENSP00000499256.2:p.Ser2701=
ENST00000700202.2:c.8101T= ENSP00000514856.2:p.Ser2701=
ENST00000700202.1:c.568T= ENSP00000514856.1:p.Ser190=
ENST00000380152.8:c.8101T= MANE Select ENSP00000369497.3:p.Ser2701=
ENST00000544455.6:c.8101T= ENSP00000439902.1:p.Ser2701=
ENST00000614259.2:c.8109T= ENSP00000506251.1:n.8109T=
ENST00000665585.1:c.666T=
ENST00000680887.1:c.8101T= ENSP00000505508.1:p.Ser2701=
ENST00000380152.7:c.8101T= ENSP00000369497.3:p.Ser2701=
ENST00000544455.5:c.8101T= ENSP00000439902.1:p.Ser2701=
NM_000059.3:c.8101T= , LRG_293t1:c.8101T= NP_000050.2:p.Ser2701=
XM_011535203.1:c.8101T= XP_011533505.1:p.Ser2701=
XM_011535204.1:c.8005T= XP_011533506.1:p.Ser2669=
XM_011535205.1:c.8101T= XP_011533507.1:p.Ser2701=
NM_000059.4:c.8101T= MANE Select NP_000050.3:p.Ser2701=