Canonical Allele Identifier: CA609453794

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2573125
• ClinVar RCV Id: RCV003315286
• dbSNP Id: rs1370021869
• gnomAD v2: 13-32912530-TGTTTG-T
• gnomAD v3: 13-32338393-TGTTTG-T
• gnomAD v4: 13-32338393-TGTTTG-T
• MyVariant Identifiers: chr13:g.32912531_32912535del (hg19) ; chr13:g.32338394_32338398del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32338394_32338398del , CM000675.2:g.32338394_32338398del	GRCh38
NC_000013.10:g.32912531_32912535del , CM000675.1:g.32912531_32912535del	GRCh37
NC_000013.9:g.31810531_31810535del	NCBI36
NG_012772.3:g.27915_27919del , LRG_293:g.27915_27919del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.4039_4043del	ENSP00000434898.2:p.Val1347TyrfsTer3
ENST00000528762.2:c.4039_4043del	ENSP00000433168.2:p.Val1347TyrfsTer3
ENST00000530893.7:c.3670_3674del	ENSP00000499438.2:p.Val1224TyrfsTer3
ENST00000665585.2:c.4039_4043del	ENSP00000499570.2:p.Val1347TyrfsTer3
ENST00000666593.2:c.4039_4043del	ENSP00000499256.2:p.Val1347TyrfsTer3
ENST00000700202.2:c.4039_4043del	ENSP00000514856.2:p.Val1347TyrfsTer3
ENST00000380152.8:c.4039_4043del MANE Select	ENSP00000369497.3:p.Val1347TyrfsTer3
ENST00000544455.6:c.4039_4043del	ENSP00000439902.1:p.Val1347TyrfsTer3
ENST00000614259.2:c.4039_4043del	ENSP00000506251.1:p.Val1347TyrfsTer3
ENST00000680887.1:c.4039_4043del	ENSP00000505508.1:p.Val1347TyrfsTer3
ENST00000380152.7:c.4039_4043del	ENSP00000369497.3:p.Val1347TyrfsTer3
ENST00000544455.5:c.4039_4043del	ENSP00000439902.1:p.Val1347TyrfsTer3
ENST00000614259.1:n.4039_4043del
NM_000059.3:c.4039_4043del , LRG_293t1:c.4039_4043del	NP_000050.2:p.Val1347TyrfsTer3
XM_011535203.1:c.4039_4043del	XP_011533505.1:p.Val1347TyrfsTer3
XM_011535204.1:c.4039_4043del	XP_011533506.1:p.Val1347TyrfsTer3
XM_011535205.1:c.4039_4043del	XP_011533507.1:p.Val1347TyrfsTer3
NM_000059.4:c.4039_4043del MANE Select	NP_000050.3:p.Val1347TyrfsTer3