Canonical Allele Identifier: CA10589019

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 266715
• ClinVar RCV Id: RCV000257888 ; RCV000509981
• dbSNP Id: rs886040441
• MyVariant Identifiers: chr13:g.32893417_32893418del (hg19) ; chr13:g.32319280_32319281del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319280_32319281del , CM000675.2:g.32319280_32319281del	GRCh38
NC_000013.10:g.32893417_32893418del , CM000675.1:g.32893417_32893418del	GRCh37
NC_000013.9:g.31791417_31791418del	NCBI36
NG_012772.3:g.8801_8802del , LRG_293:g.8801_8802del
NG_017006.2:g.1083_1084del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.271_272del	ENSP00000434898.2:p.Tyr91ProfsTer9
ENST00000528762.2:c.271_272del	ENSP00000433168.2:p.Tyr91ProfsTer9
ENST00000530893.7:c.-99_-98del	ENSP00000499438.2:n.-99_-98del
ENST00000665585.2:c.271_272del	ENSP00000499570.2:p.Tyr91ProfsTer9
ENST00000666593.2:c.271_272del	ENSP00000499256.2:p.Tyr91ProfsTer9
ENST00000700202.2:c.271_272del	ENSP00000514856.2:p.Tyr91ProfsTer9
ENST00000700200.1:n.191+2753_191+2754del
ENST00000700201.1:c.271_272del	ENSP00000514855.1:p.Tyr91ProfsTer9
ENST00000380152.8:c.271_272del MANE Select	ENSP00000369497.3:p.Tyr91ProfsTer9
ENST00000544455.6:c.271_272del	ENSP00000439902.1:p.Tyr91ProfsTer9
ENST00000614259.2:c.271_272del	ENSP00000506251.1:p.Tyr91ProfsTer9
ENST00000680887.1:c.271_272del	ENSP00000505508.1:p.Tyr91ProfsTer9
ENST00000380152.7:c.271_272del	ENSP00000369497.3:p.Tyr91ProfsTer9
ENST00000530893.6:n.469_470del
ENST00000544455.5:c.271_272del	ENSP00000439902.1:p.Tyr91ProfsTer9
ENST00000614259.1:n.271_272del
NM_000059.3:c.271_272del , LRG_293t1:c.271_272del	NP_000050.2:p.Tyr91ProfsTer9
XM_011535203.1:c.271_272del	XP_011533505.1:p.Tyr91ProfsTer9
XM_011535204.1:c.271_272del	XP_011533506.1:p.Tyr91ProfsTer9
XM_011535205.1:c.271_272del	XP_011533507.1:p.Tyr91ProfsTer9
NM_000059.4:c.271_272del MANE Select	NP_000050.3:p.Tyr91ProfsTer9