Canonical Allele Identifier: CA2580087327
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759825
ClinVar RCV Id: RCV002396243

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32357740_32357767delinsGTGTTATTTTGTTTTATT , CM000675.2:g.32357740_32357767delinsGTGTTATTTTGTTTTATT GRCh38
NC_000013.10:g.32931877_32931904delinsGTGTTATTTTGTTTTATT , CM000675.1:g.32931877_32931904delinsGTGTTATTTTGTTTTATT GRCh37
NC_000013.9:g.31829877_31829904delinsGTGTTATTTTGTTTTATT NCBI36
NG_012772.3:g.47261_47288delinsGTGTTATTTTGTTTTATT , LRG_293:g.47261_47288delinsGTGTTATTTTGTTTTATT

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000528762.2:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000530893.7:c.7249-2_7274delinsGTGTTATTTTGTTTTATT
ENST00000665585.2:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000666593.2:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000700202.2:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000700202.1:c.85-2_110delinsGTGTTATTTTGTTTTATT
ENST00000380152.8:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000544455.6:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000614259.2:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000665585.1:c.183-2_208delinsGTGTTATTTTGTTTTATT
ENST00000680887.1:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000380152.7:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000544455.5:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
ENST00000614259.1:n.7618-2_7643delinsGTGTTATTTTGTTTTATT
NM_000059.3:c.7618-2_7643delinsGTGTTATTTTGTTTTATT , LRG_293t1:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
XM_011535203.1:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
XM_011535204.1:c.7522-2_7547delinsGTGTTATTTTGTTTTATT
XM_011535205.1:c.7618-2_7643delinsGTGTTATTTTGTTTTATT
NM_000059.4:c.7618-2_7643delinsGTGTTATTTTGTTTTATT