Canonical Allele Identifier: CA658798122

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 531366
• ClinVar RCV Id: RCV000637655 ; RCV000985551 ; RCV001186731 ; RCV003451523
• dbSNP Id: rs1555284412
• MyVariant Identifiers: chr13:g.32914318_32914319del (hg19) ; chr13:g.32340181_32340182del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340181_32340182del , CM000675.2:g.32340181_32340182del	GRCh38
NC_000013.10:g.32914318_32914319del , CM000675.1:g.32914318_32914319del	GRCh37
NC_000013.9:g.31812318_31812319del	NCBI36
NG_012772.3:g.29702_29703del , LRG_293:g.29702_29703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.5826_5827del	ENSP00000434898.2:p.Ser1943Ter
ENST00000528762.2:c.5826_5827del	ENSP00000433168.2:p.Ser1943Ter
ENST00000530893.7:c.5457_5458del	ENSP00000499438.2:p.Ser1820Ter
ENST00000665585.2:c.5826_5827del	ENSP00000499570.2:p.Ser1943Ter
ENST00000666593.2:c.5826_5827del	ENSP00000499256.2:p.Ser1943Ter
ENST00000700202.2:c.5826_5827del	ENSP00000514856.2:p.Ser1943Ter
ENST00000380152.8:c.5826_5827del MANE Select	ENSP00000369497.3:p.Ser1943Ter
ENST00000544455.6:c.5826_5827del	ENSP00000439902.1:p.Ser1943Ter
ENST00000614259.2:c.5826_5827del	ENSP00000506251.1:p.Ser1943Ter
ENST00000680887.1:c.5826_5827del	ENSP00000505508.1:p.Ser1943Ter
ENST00000380152.7:c.5826_5827del	ENSP00000369497.3:p.Ser1943Ter
ENST00000544455.5:c.5826_5827del	ENSP00000439902.1:p.Ser1943Ter
ENST00000614259.1:n.5826_5827del
NM_000059.3:c.5826_5827del , LRG_293t1:c.5826_5827del	NP_000050.2:p.Ser1943Ter
XM_011535203.1:c.5826_5827del	XP_011533505.1:p.Ser1943Ter
XM_011535204.1:c.5826_5827del	XP_011533506.1:p.Ser1943Ter
XM_011535205.1:c.5826_5827del	XP_011533507.1:p.Ser1943Ter
NM_000059.4:c.5826_5827del MANE Select	NP_000050.3:p.Ser1943Ter