Canonical Allele Identifier: CA2082819193
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32341277_32341280del , CM000675.2:g.32341277_32341280del GRCh38
NC_000013.10:g.32915414_32915417del , CM000675.1:g.32915414_32915417del GRCh37
NC_000013.9:g.31813414_31813417del NCBI36
NG_012772.3:g.30798_30801del , LRG_293:g.30798_30801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.6841+81_6841+84del ENSP00000434898.2:n.6841+81_6841+84del
ENST00000528762.2:c.6841+81_6841+84del ENSP00000433168.2:n.6841+81_6841+84del
ENST00000530893.7:c.6472+81_6472+84del ENSP00000499438.2:n.6472+81_6472+84del
ENST00000665585.2:c.6841+81_6841+84del ENSP00000499570.2:n.6841+81_6841+84del
ENST00000666593.2:c.6841+81_6841+84del ENSP00000499256.2:n.6841+81_6841+84del
ENST00000700202.2:c.6841+81_6841+84del ENSP00000514856.2:n.6841+81_6841+84del
ENST00000380152.8:c.6841+81_6841+84del MANE Select ENSP00000369497.3:n.6841+81_6841+84del
ENST00000544455.6:c.6841+81_6841+84del ENSP00000439902.1:n.6841+81_6841+84del
ENST00000614259.2:c.6841+81_6841+84del ENSP00000506251.1:n.6841+81_6841+84del
ENST00000680887.1:c.6841+81_6841+84del ENSP00000505508.1:n.6841+81_6841+84del
ENST00000380152.7:c.6841+81_6841+84del ENSP00000369497.3:n.6841+81_6841+84del
ENST00000544455.5:c.6841+81_6841+84del ENSP00000439902.1:n.6841+81_6841+84del
ENST00000614259.1:n.6841+81_6841+84del
NM_000059.3:c.6841+81_6841+84del , LRG_293t1:c.6841+81_6841+84del NP_000050.2:n.6841+81_6841+84del
XM_011535203.1:c.6841+81_6841+84del XP_011533505.1:n.6841+81_6841+84del
XM_011535204.1:c.6841+81_6841+84del XP_011533506.1:n.6841+81_6841+84del
XM_011535205.1:c.6841+81_6841+84del XP_011533507.1:n.6841+81_6841+84del
NM_000059.4:c.6841+81_6841+84del MANE Select NP_000050.3:n.6841+81_6841+84del