Canonical Allele Identifier: CA16613896

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 409464
• ClinVar RCV Id: RCV000456555 ; RCV000661737
• dbSNP Id: rs1064792960
• MyVariant Identifiers: chr13:g.32893349_32893364del (hg19) ; chr13:g.32319212_32319227del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319212_32319227del , CM000675.2:g.32319212_32319227del	GRCh38
NC_000013.10:g.32893349_32893364del , CM000675.1:g.32893349_32893364del	GRCh37
NC_000013.9:g.31791349_31791364del	NCBI36
NG_012772.3:g.8733_8748del , LRG_293:g.8733_8748del
NG_017006.2:g.1138_1153del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.203_218del	ENSP00000434898.2:p.Lys68SerfsTer7
ENST00000528762.2:c.203_218del	ENSP00000433168.2:p.Lys68SerfsTer7
ENST00000530893.7:c.-167_-152del	ENSP00000499438.2:n.-167_-152del
ENST00000665585.2:c.203_218del	ENSP00000499570.2:p.Lys68SerfsTer7
ENST00000666593.2:c.203_218del	ENSP00000499256.2:p.Lys68SerfsTer7
ENST00000700202.2:c.203_218del	ENSP00000514856.2:p.Lys68SerfsTer7
ENST00000700200.1:n.191+2685_191+2700del
ENST00000700201.1:c.203_218del	ENSP00000514855.1:p.Lys68SerfsTer7
ENST00000380152.8:c.203_218del MANE Select	ENSP00000369497.3:p.Lys68SerfsTer7
ENST00000544455.6:c.203_218del	ENSP00000439902.1:p.Lys68SerfsTer7
ENST00000614259.2:c.203_218del	ENSP00000506251.1:p.Lys68SerfsTer7
ENST00000680887.1:c.203_218del	ENSP00000505508.1:p.Lys68SerfsTer7
ENST00000380152.7:c.203_218del	ENSP00000369497.3:p.Lys68SerfsTer7
ENST00000530893.6:n.401_416del
ENST00000544455.5:c.203_218del	ENSP00000439902.1:p.Lys68SerfsTer7
ENST00000614259.1:n.203_218del
NM_000059.3:c.203_218del , LRG_293t1:c.203_218del	NP_000050.2:p.Lys68SerfsTer7
XM_011535203.1:c.203_218del	XP_011533505.1:p.Lys68SerfsTer7
XM_011535204.1:c.203_218del	XP_011533506.1:p.Lys68SerfsTer7
XM_011535205.1:c.203_218del	XP_011533507.1:p.Lys68SerfsTer7
NM_000059.4:c.203_218del MANE Select	NP_000050.3:p.Lys68SerfsTer7