Canonical Allele Identifier: CA014707

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 141961
• ClinVar RCV Id: RCV000130703 ; RCV000160045 ; RCV000197517 ; RCV000410547 ; RCV000985472
• dbSNP Id: rs374691587
• ExAC: 13:32910725 A / G
• gnomAD v2: 13-32910725-A-G
• gnomAD v3: 13-32336588-A-G
• gnomAD v4: 13-32336588-A-G
• MyVariant Identifiers: chr13:g.32910725A>G (hg19) ; chr13:g.32336588A>G (hg38)
• PubMed: PMID:18284688 ; PMID:22034289

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32336588A>G , CM000675.2:g.32336588A>G	GRCh38
NC_000013.10:g.32910725A>G , CM000675.1:g.32910725A>G	GRCh37
NC_000013.9:g.31808725A>G	NCBI36
NG_012772.3:g.26109A>G , LRG_293:g.26109A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2233A>G	ENSP00000434898.2:p.Lys745Glu
ENST00000528762.2:c.2233A>G	ENSP00000433168.2:p.Lys745Glu
ENST00000530893.7:c.1864A>G	ENSP00000499438.2:p.Lys622Glu
ENST00000665585.2:c.2233A>G	ENSP00000499570.2:p.Lys745Glu
ENST00000666593.2:c.2233A>G	ENSP00000499256.2:p.Lys745Glu
ENST00000700202.2:c.2233A>G	ENSP00000514856.2:p.Lys745Glu
ENST00000380152.8:c.2233A>G MANE Select	ENSP00000369497.3:p.Lys745Glu
ENST00000544455.6:c.2233A>G	ENSP00000439902.1:p.Lys745Glu
ENST00000614259.2:c.2233A>G	ENSP00000506251.1:p.Lys745Glu
ENST00000680887.1:c.2233A>G	ENSP00000505508.1:p.Lys745Glu
ENST00000380152.7:c.2233A>G	ENSP00000369497.3:p.Lys745Glu
ENST00000544455.5:c.2233A>G	ENSP00000439902.1:p.Lys745Glu
ENST00000614259.1:n.2233A>G
NM_000059.3:c.2233A>G , LRG_293t1:c.2233A>G	NP_000050.2:p.Lys745Glu
XM_011535203.1:c.2233A>G	XP_011533505.1:p.Lys745Glu
XM_011535204.1:c.2233A>G	XP_011533506.1:p.Lys745Glu
XM_011535205.1:c.2233A>G	XP_011533507.1:p.Lys745Glu
NM_000059.4:c.2233A>G MANE Select	NP_000050.3:p.Lys745Glu