Canonical Allele Identifier: CA2082835360
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32363306G= , CM000675.2:g.32363306G= GRCh38
NC_000013.10:g.32937443G= , CM000675.1:g.32937443G= GRCh37
NC_000013.9:g.31835443G= NCBI36
NG_012772.3:g.52827G= , LRG_293:g.52827G=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8104G= ENSP00000434898.2:p.Glu2702=
ENST00000528762.2:c.8104G= ENSP00000433168.2:p.Glu2702=
ENST00000530893.7:c.7735G= ENSP00000499438.2:p.Glu2579=
ENST00000665585.2:c.8104G= ENSP00000499570.2:p.Glu2702=
ENST00000666593.2:c.8104G= ENSP00000499256.2:p.Glu2702=
ENST00000700202.2:c.8104G= ENSP00000514856.2:p.Glu2702=
ENST00000700202.1:c.571G= ENSP00000514856.1:p.Glu191=
ENST00000380152.8:c.8104G= MANE Select ENSP00000369497.3:p.Glu2702=
ENST00000544455.6:c.8104G= ENSP00000439902.1:p.Glu2702=
ENST00000614259.2:c.8112G= ENSP00000506251.1:n.8112G=
ENST00000665585.1:c.669G=
ENST00000680887.1:c.8104G= ENSP00000505508.1:p.Glu2702=
ENST00000380152.7:c.8104G= ENSP00000369497.3:p.Glu2702=
ENST00000544455.5:c.8104G= ENSP00000439902.1:p.Glu2702=
NM_000059.3:c.8104G= , LRG_293t1:c.8104G= NP_000050.2:p.Glu2702=
XM_011535203.1:c.8104G= XP_011533505.1:p.Glu2702=
XM_011535204.1:c.8008G= XP_011533506.1:p.Glu2670=
XM_011535205.1:c.8104G= XP_011533507.1:p.Glu2702=
NM_000059.4:c.8104G= MANE Select NP_000050.3:p.Glu2702=