Canonical Allele Identifier: CA2082809282
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32355003_32355005delinsCAA , CM000675.2:g.32355003_32355005delinsCAA GRCh38
NC_000013.10:g.32929140_32929142delinsCAA , CM000675.1:g.32929140_32929142delinsCAA GRCh37
NC_000013.9:g.31827140_31827142delinsCAA NCBI36
NG_012772.3:g.44524_44526delinsCAA , LRG_293:g.44524_44526delinsCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7150_7152delinsCAA ENSP00000434898.2:p.Gln2384=
ENST00000528762.2:c.7150_7152delinsCAA ENSP00000433168.2:p.Gln2384=
ENST00000530893.7:c.6781_6783delinsCAA ENSP00000499438.2:p.Gln2261=
ENST00000665585.2:c.7150_7152delinsCAA ENSP00000499570.2:p.Gln2384=
ENST00000666593.2:c.7150_7152delinsCAA ENSP00000499256.2:p.Gln2384=
ENST00000700202.2:c.7150_7152delinsCAA ENSP00000514856.2:p.Gln2384=
ENST00000380152.8:c.7150_7152delinsCAA MANE Select ENSP00000369497.3:p.Gln2384=
ENST00000544455.6:c.7150_7152delinsCAA ENSP00000439902.1:p.Gln2384=
ENST00000614259.2:c.7150_7152delinsCAA ENSP00000506251.1:p.Gln2384=
ENST00000680887.1:c.7150_7152delinsCAA ENSP00000505508.1:p.Gln2384=
ENST00000380152.7:c.7150_7152delinsCAA ENSP00000369497.3:p.Gln2384=
ENST00000544455.5:c.7150_7152delinsCAA ENSP00000439902.1:p.Gln2384=
ENST00000614259.1:n.7150_7152delinsCAA
NM_000059.3:c.7150_7152delinsCAA , LRG_293t1:c.7150_7152delinsCAA NP_000050.2:p.Gln2384=
XM_011535203.1:c.7150_7152delinsCAA XP_011533505.1:p.Gln2384=
XM_011535204.1:c.7054_7056delinsCAA XP_011533506.1:p.Gln2352=
XM_011535205.1:c.7150_7152delinsCAA XP_011533507.1:p.Gln2384=
NM_000059.4:c.7150_7152delinsCAA MANE Select NP_000050.3:p.Gln2384=