Canonical Allele Identifier: CA10589436

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 267019
• ClinVar RCV Id: RCV002392786
• dbSNP Id: rs886040715
• MyVariant Identifiers: chr13:g.32930659_32930660del (hg19) ; chr13:g.32356522_32356523del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32356522_32356523del , CM000675.2:g.32356522_32356523del	GRCh38
NC_000013.10:g.32930659_32930660del , CM000675.1:g.32930659_32930660del	GRCh37
NC_000013.9:g.31828659_31828660del	NCBI36
NG_012772.3:g.46043_46044del , LRG_293:g.46043_46044del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7530_7531del	ENSP00000434898.2:p.Tyr2511SerfsTer27
ENST00000528762.2:c.7530_7531del	ENSP00000433168.2:p.Tyr2511SerfsTer27
ENST00000530893.7:c.7161_7162del	ENSP00000499438.2:p.Tyr2388SerfsTer27
ENST00000665585.2:c.7530_7531del	ENSP00000499570.2:p.Tyr2511SerfsTer27
ENST00000666593.2:c.7530_7531del	ENSP00000499256.2:p.Tyr2511SerfsTer27
ENST00000700202.2:c.7530_7531del	ENSP00000514856.2:p.Tyr2511SerfsTer27
ENST00000380152.8:c.7530_7531del MANE Select	ENSP00000369497.3:p.Tyr2511SerfsTer27
ENST00000544455.6:c.7530_7531del	ENSP00000439902.1:p.Tyr2511SerfsTer27
ENST00000614259.2:c.7530_7531del	ENSP00000506251.1:p.Tyr2511SerfsTer27
ENST00000665585.1:c.95_96del
ENST00000680887.1:c.7530_7531del	ENSP00000505508.1:p.Tyr2511SerfsTer27
ENST00000380152.7:c.7530_7531del	ENSP00000369497.3:p.Tyr2511SerfsTer27
ENST00000544455.5:c.7530_7531del	ENSP00000439902.1:p.Tyr2511SerfsTer27
ENST00000614259.1:n.7530_7531del
NM_000059.3:c.7530_7531del , LRG_293t1:c.7530_7531del	NP_000050.2:p.Tyr2511SerfsTer27
XM_011535203.1:c.7530_7531del	XP_011533505.1:p.Tyr2511SerfsTer27
XM_011535204.1:c.7434_7435del	XP_011533506.1:p.Tyr2479SerfsTer27
XM_011535205.1:c.7530_7531del	XP_011533507.1:p.Tyr2511SerfsTer27
NM_000059.4:c.7530_7531del MANE Select	NP_000050.3:p.Tyr2511SerfsTer27