Canonical Allele Identifier: CA10589313

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 266876
• ClinVar RCV Id: RCV000257666
• dbSNP Id: rs886040591
• MyVariant Identifiers: chr13:g.32913934_32913937dupGACT (hg19) ; chr13:g.32339797_32339800dupGACT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339797_32339800dup , CM000675.2:g.32339797_32339800dup	GRCh38
NC_000013.10:g.32913934_32913937dup , CM000675.1:g.32913934_32913937dup	GRCh37
NC_000013.9:g.31811934_31811937dup	NCBI36
NG_012772.3:g.29318_29321dup , LRG_293:g.29318_29321dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.5442_5445dup	ENSP00000434898.2:p.Ser1816AspfsTer2
ENST00000528762.2:c.5442_5445dup	ENSP00000433168.2:p.Ser1816AspfsTer2
ENST00000530893.7:c.5073_5076dup	ENSP00000499438.2:p.Ser1693AspfsTer2
ENST00000665585.2:c.5442_5445dup	ENSP00000499570.2:p.Ser1816AspfsTer2
ENST00000666593.2:c.5442_5445dup	ENSP00000499256.2:p.Ser1816AspfsTer2
ENST00000700202.2:c.5442_5445dup	ENSP00000514856.2:p.Ser1816AspfsTer2
ENST00000380152.8:c.5442_5445dup MANE Select	ENSP00000369497.3:p.Ser1816AspfsTer2
ENST00000544455.6:c.5442_5445dup	ENSP00000439902.1:p.Ser1816AspfsTer2
ENST00000614259.2:c.5442_5445dup	ENSP00000506251.1:p.Ser1816AspfsTer2
ENST00000680887.1:c.5442_5445dup	ENSP00000505508.1:p.Ser1816AspfsTer2
ENST00000380152.7:c.5442_5445dup	ENSP00000369497.3:p.Ser1816AspfsTer2
ENST00000544455.5:c.5442_5445dup	ENSP00000439902.1:p.Ser1816AspfsTer2
ENST00000614259.1:n.5442_5445dup
NM_000059.3:c.5442_5445dup , LRG_293t1:c.5442_5445dup	NP_000050.2:p.Ser1816AspfsTer2
XM_011535203.1:c.5442_5445dup	XP_011533505.1:p.Ser1816AspfsTer2
XM_011535204.1:c.5442_5445dup	XP_011533506.1:p.Ser1816AspfsTer2
XM_011535205.1:c.5442_5445dup	XP_011533507.1:p.Ser1816AspfsTer2
NM_000059.4:c.5442_5445dup MANE Select	NP_000050.3:p.Ser1816AspfsTer2