Canonical Allele Identifier: CA891866564

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32893422_32898491del (hg19) ; chr13:g.32319285_32324354del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319285_32324354del , CM000675.2:g.32319285_32324354del	GRCh38
NC_000013.10:g.32893422_32898491del , CM000675.1:g.32893422_32898491del	GRCh37
NC_000013.9:g.31791422_31796491del	NCBI36
NG_012772.3:g.8806_13875del , LRG_293:g.8806_13875del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.276_317-722del
ENST00000528762.2:c.276_317-722del
ENST00000530893.7:c.-94_-53-722del
ENST00000665585.2:c.276_317-722del
ENST00000666593.2:c.276_317-722del
ENST00000700202.2:c.276_317-722del
ENST00000700200.1:n.191+2758_192-726del
ENST00000700201.1:c.276_317-304del
ENST00000380152.8:c.276_317-722del
ENST00000544455.6:c.276_317-722del
ENST00000614259.2:c.276_317-722del
ENST00000680887.1:c.276_317-722del
ENST00000380152.7:c.276_317-722del
ENST00000530893.6:n.474_515-722del
ENST00000544455.5:c.276_317-722del
ENST00000614259.1:n.276_317-722del
NM_000059.3:c.276_317-722del , LRG_293t1:c.276_317-722del
XM_011535203.1:c.276_317-722del
XM_011535204.1:c.276_317-722del
XM_011535205.1:c.276_317-722del
NM_000059.4:c.276_317-722del