Canonical Allele Identifier: CA2082821823
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394691C= , CM000675.2:g.32394691C= GRCh38
NC_000013.10:g.32968828C= , CM000675.1:g.32968828C= GRCh37
NC_000013.9:g.31866828C= NCBI36
NG_012772.3:g.84212C= , LRG_293:g.84212C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.9259C= ENSP00000434898.2:p.Leu3087=
ENST00000528762.2:c.*626C= ENSP00000433168.2:n.*626C=
ENST00000530893.7:c.8890C= ENSP00000499438.2:p.Leu2964=
ENST00000665585.2:c.*821C= ENSP00000499570.2:n.*821C=
ENST00000666593.2:c.*104C= ENSP00000499256.2:n.*104C=
ENST00000700202.2:c.9208C= ENSP00000514856.2:p.Leu3070=
ENST00000700202.1:c.1675C= ENSP00000514856.1:p.Leu559=
ENST00000700203.1:n.1386C=
ENST00000380152.8:c.9259C= MANE Select ENSP00000369497.3:p.Leu3087=
ENST00000544455.6:c.9259C= ENSP00000439902.1:p.Leu3087=
ENST00000614259.2:c.9267C= ENSP00000506251.1:n.9267C=
ENST00000665585.1:c.2137C=
ENST00000666593.1:c.281C= ENSP00000499256.1:n.281C=
ENST00000680887.1:c.9259C= ENSP00000505508.1:p.Leu3087=
ENST00000380152.7:c.9259C= ENSP00000369497.3:p.Leu3087=
ENST00000470094.1:c.216C=
ENST00000544455.5:c.9259C= ENSP00000439902.1:p.Leu3087=
NM_000059.3:c.9259C= , LRG_293t1:c.9259C= NP_000050.2:p.Leu3087=
XM_011535203.1:c.9259C= XP_011533505.1:p.Leu3087=
XM_011535204.1:c.9163C= XP_011533506.1:p.Leu3055=
NM_000059.4:c.9259C= MANE Select NP_000050.3:p.Leu3087=