Canonical Allele Identifier: CA011902

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 91751
• ClinVar RCV Id: RCV000077659 ; RCV000546238
• dbSNP Id: rs398122726
• MyVariant Identifiers: chr13:g.32907014_32907017del (hg19) ; chr13:g.32332877_32332880del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32332877_32332880del , CM000675.2:g.32332877_32332880del	GRCh38
NC_000013.10:g.32907014_32907017del , CM000675.1:g.32907014_32907017del	GRCh37
NC_000013.9:g.31805014_31805017del	NCBI36
NG_012772.3:g.22398_22401del , LRG_293:g.22398_22401del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.1399_1402del	ENSP00000434898.2:p.Lys467GlufsTer17
ENST00000528762.2:c.1399_1402del	ENSP00000433168.2:p.Lys467GlufsTer17
ENST00000530893.7:c.1030_1033del	ENSP00000499438.2:p.Lys344GlufsTer17
ENST00000665585.2:c.1399_1402del	ENSP00000499570.2:p.Lys467GlufsTer17
ENST00000666593.2:c.1399_1402del	ENSP00000499256.2:p.Lys467GlufsTer17
ENST00000700202.2:c.1399_1402del	ENSP00000514856.2:p.Lys467GlufsTer17
ENST00000700201.1:c.*1178_*1181del	ENSP00000514855.1:n.*1178_*1181del
ENST00000380152.8:c.1399_1402del MANE Select	ENSP00000369497.3:p.Lys467GlufsTer17
ENST00000544455.6:c.1399_1402del	ENSP00000439902.1:p.Lys467GlufsTer17
ENST00000614259.2:c.1399_1402del	ENSP00000506251.1:p.Lys467GlufsTer17
ENST00000680887.1:c.1399_1402del	ENSP00000505508.1:p.Lys467GlufsTer17
ENST00000380152.7:c.1399_1402del	ENSP00000369497.3:p.Lys467GlufsTer17
ENST00000530893.6:n.1597_1600del
ENST00000544455.5:c.1399_1402del	ENSP00000439902.1:p.Lys467GlufsTer17
ENST00000614259.1:n.1399_1402del
NM_000059.3:c.1399_1402del , LRG_293t1:c.1399_1402del	NP_000050.2:p.Lys467GlufsTer17
XM_011535203.1:c.1399_1402del	XP_011533505.1:p.Lys467GlufsTer17
XM_011535204.1:c.1399_1402del	XP_011533506.1:p.Lys467GlufsTer17
XM_011535205.1:c.1399_1402del	XP_011533507.1:p.Lys467GlufsTer17
NM_000059.4:c.1399_1402del MANE Select	NP_000050.3:p.Lys467GlufsTer17