Canonical Allele Identifier: CA2082772893
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32333382_32333387delinsATTCAG , CM000675.2:g.32333382_32333387delinsATTCAG GRCh38
NC_000013.10:g.32907519_32907524delinsATTCAG , CM000675.1:g.32907519_32907524delinsATTCAG GRCh37
NC_000013.9:g.31805519_31805524delinsATTCAG NCBI36
NG_012772.3:g.22903_22908delinsATTCAG , LRG_293:g.22903_22908delinsATTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1904_1909delinsATTCAG ENSP00000434898.2:p.Asp635=
ENST00000528762.2:c.1904_1909delinsATTCAG ENSP00000433168.2:p.Asp635=
ENST00000530893.7:c.1535_1540delinsATTCAG ENSP00000499438.2:p.Asp512=
ENST00000665585.2:c.1904_1909delinsATTCAG ENSP00000499570.2:p.Asp635=
ENST00000666593.2:c.1904_1909delinsATTCAG ENSP00000499256.2:p.Asp635=
ENST00000700202.2:c.1904_1909delinsATTCAG ENSP00000514856.2:p.Asp635=
ENST00000380152.8:c.1904_1909delinsATTCAG MANE Select ENSP00000369497.3:p.Asp635=
ENST00000544455.6:c.1904_1909delinsATTCAG ENSP00000439902.1:p.Asp635=
ENST00000614259.2:c.1904_1909delinsATTCAG ENSP00000506251.1:p.Asp635=
ENST00000680887.1:c.1904_1909delinsATTCAG ENSP00000505508.1:p.Asp635=
ENST00000380152.7:c.1904_1909delinsATTCAG ENSP00000369497.3:p.Asp635=
ENST00000544455.5:c.1904_1909delinsATTCAG ENSP00000439902.1:p.Asp635=
ENST00000614259.1:n.1904_1909delinsATTCAG
NM_000059.3:c.1904_1909delinsATTCAG , LRG_293t1:c.1904_1909delinsATTCAG NP_000050.2:p.Asp635=
XM_011535203.1:c.1904_1909delinsATTCAG XP_011533505.1:p.Asp635=
XM_011535204.1:c.1904_1909delinsATTCAG XP_011533506.1:p.Asp635=
XM_011535205.1:c.1904_1909delinsATTCAG XP_011533507.1:p.Asp635=
NM_000059.4:c.1904_1909delinsATTCAG MANE Select NP_000050.3:p.Asp635=