Canonical Allele Identifier: CA2082775415
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32316444G= , CM000675.2:g.32316444G= GRCh38
NC_000013.10:g.32890581G= , CM000675.1:g.32890581G= GRCh37
NC_000013.9:g.31788581G= NCBI36
NG_012772.3:g.5965G= , LRG_293:g.5965G=
NG_017006.1:g.511C=
NG_017006.2:g.3920C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.-17G= ENSP00000434898.2:n.-17G=
ENST00000528762.2:c.-17G= ENSP00000433168.2:n.-17G=
ENST00000530893.7:c.-382G= ENSP00000499438.2:n.-382G=
ENST00000665585.2:c.-17G= ENSP00000499570.2:n.-17G=
ENST00000666593.2:c.-17G= ENSP00000499256.2:n.-17G=
ENST00000700202.2:c.-17G= ENSP00000514856.2:n.-17G=
ENST00000700199.1:n.108G=
ENST00000700200.1:n.108G=
ENST00000700201.1:c.-17G= ENSP00000514855.1:n.-17G=
ENST00000380152.8:c.-17G= MANE Select ENSP00000369497.3:n.-17G=
ENST00000544455.6:c.-17G= ENSP00000439902.1:n.-17G=
ENST00000680887.1:c.-17G= ENSP00000505508.1:n.-17G=
ENST00000380152.7:c.-17G= ENSP00000369497.3:n.-17G=
ENST00000530893.6:n.186G=
ENST00000544455.5:c.-17G= ENSP00000439902.1:n.-17G=
NM_000059.3:c.-17G= , LRG_293t1:c.-17G= NP_000050.2:n.-17G=
XM_011535203.1:c.-17G= XP_011533505.1:n.-17G=
XM_011535204.1:c.-17G= XP_011533506.1:n.-17G=
XM_011535205.1:c.-17G= XP_011533507.1:n.-17G=
NM_000059.4:c.-17G= MANE Select NP_000050.3:n.-17G=