Canonical Allele Identifier: CA2082819151
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32341273_32341277delinsCAATT , CM000675.2:g.32341273_32341277delinsCAATT GRCh38
NC_000013.10:g.32915410_32915414delinsCAATT , CM000675.1:g.32915410_32915414delinsCAATT GRCh37
NC_000013.9:g.31813410_31813414delinsCAATT NCBI36
NG_012772.3:g.30794_30798delinsCAATT , LRG_293:g.30794_30798delinsCAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.6841+77_6841+81delinsCAATT ENSP00000434898.2:n.6841+77_6841+81delinsCAATT
ENST00000528762.2:c.6841+77_6841+81delinsCAATT ENSP00000433168.2:n.6841+77_6841+81delinsCAATT
ENST00000530893.7:c.6472+77_6472+81delinsCAATT ENSP00000499438.2:n.6472+77_6472+81delinsCAATT
ENST00000665585.2:c.6841+77_6841+81delinsCAATT ENSP00000499570.2:n.6841+77_6841+81delinsCAATT
ENST00000666593.2:c.6841+77_6841+81delinsCAATT ENSP00000499256.2:n.6841+77_6841+81delinsCAATT
ENST00000700202.2:c.6841+77_6841+81delinsCAATT ENSP00000514856.2:n.6841+77_6841+81delinsCAATT
ENST00000380152.8:c.6841+77_6841+81delinsCAATT MANE Select ENSP00000369497.3:n.6841+77_6841+81delinsCAATT
ENST00000544455.6:c.6841+77_6841+81delinsCAATT ENSP00000439902.1:n.6841+77_6841+81delinsCAATT
ENST00000614259.2:c.6841+77_6841+81delinsCAATT ENSP00000506251.1:n.6841+77_6841+81delinsCAATT
ENST00000680887.1:c.6841+77_6841+81delinsCAATT ENSP00000505508.1:n.6841+77_6841+81delinsCAATT
ENST00000380152.7:c.6841+77_6841+81delinsCAATT ENSP00000369497.3:n.6841+77_6841+81delinsCAATT
ENST00000544455.5:c.6841+77_6841+81delinsCAATT ENSP00000439902.1:n.6841+77_6841+81delinsCAATT
ENST00000614259.1:n.6841+77_6841+81delinsCAATT
NM_000059.3:c.6841+77_6841+81delinsCAATT , LRG_293t1:c.6841+77_6841+81delinsCAATT NP_000050.2:n.6841+77_6841+81delinsCAATT
XM_011535203.1:c.6841+77_6841+81delinsCAATT XP_011533505.1:n.6841+77_6841+81delinsCAATT
XM_011535204.1:c.6841+77_6841+81delinsCAATT XP_011533506.1:n.6841+77_6841+81delinsCAATT
XM_011535205.1:c.6841+77_6841+81delinsCAATT XP_011533507.1:n.6841+77_6841+81delinsCAATT
NM_000059.4:c.6841+77_6841+81delinsCAATT MANE Select NP_000050.3:n.6841+77_6841+81delinsCAATT