Canonical Allele Identifier: CA915943610

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 810853
• ClinVar RCV Id: RCV001000111

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319286_32324350delinsCCAT , CM000675.2:g.32319286_32324350delinsCCAT	GRCh38
NC_000013.10:g.32893423_32898487delinsCCAT , CM000675.1:g.32893423_32898487delinsCCAT	GRCh37
NC_000013.9:g.31791423_31796487delinsCCAT	NCBI36
NG_012772.3:g.8807_13871delinsCCAT , LRG_293:g.8807_13871delinsCCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.277_317-726delinsCCAT
ENST00000528762.2:c.277_317-726delinsCCAT
ENST00000530893.7:c.-93_-53-726delinsCCAT
ENST00000665585.2:c.277_317-726delinsCCAT
ENST00000666593.2:c.277_317-726delinsCCAT
ENST00000700202.2:c.277_317-726delinsCCAT
ENST00000700200.1:n.191+2759_192-730delinsCCAT
ENST00000700201.1:c.277_317-308delinsCCAT
ENST00000380152.8:c.277_317-726delinsCCAT
ENST00000544455.6:c.277_317-726delinsCCAT
ENST00000614259.2:c.277_317-726delinsCCAT
ENST00000680887.1:c.277_317-726delinsCCAT
ENST00000380152.7:c.277_317-726delinsCCAT
ENST00000530893.6:n.475_515-726delinsCCAT
ENST00000544455.5:c.277_317-726delinsCCAT
ENST00000614259.1:n.277_317-726delinsCCAT
NM_000059.3:c.277_317-726delinsCCAT , LRG_293t1:c.277_317-726delinsCCAT
XM_011535203.1:c.277_317-726delinsCCAT
XM_011535204.1:c.277_317-726delinsCCAT
XM_011535205.1:c.277_317-726delinsCCAT
NM_000059.4:c.277_317-726delinsCCAT