Canonical Allele Identifier: CA021240

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 51765
• ClinVar RCV Id: RCV000044553 ; RCV000113377 ; RCV000130603 ; RCV000587656 ; RCV001175365
• dbSNP Id: rs80358732
• ExAC: 13:32913588 A / G
• gnomAD v2: 13-32913588-A-G
• gnomAD v3: 13-32339451-A-G
• gnomAD v4: 13-32339451-A-G
• MyVariant Identifiers: chr13:g.32913588A>G (hg19) ; chr13:g.32339451A>G (hg38)
• PubMed: PMID:10923033 ; PMID:19912264 ; PMID:23192404 ; PMID:26689913 ; PMID:27223485

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339451A>G , CM000675.2:g.32339451A>G	GRCh38
NC_000013.10:g.32913588A>G , CM000675.1:g.32913588A>G	GRCh37
NC_000013.9:g.31811588A>G	NCBI36
NG_012772.3:g.28972A>G , LRG_293:g.28972A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.5096A>G	ENSP00000434898.2:p.Asp1699Gly
ENST00000528762.2:c.5096A>G	ENSP00000433168.2:p.Asp1699Gly
ENST00000530893.7:c.4727A>G	ENSP00000499438.2:p.Asp1576Gly
ENST00000665585.2:c.5096A>G	ENSP00000499570.2:p.Asp1699Gly
ENST00000666593.2:c.5096A>G	ENSP00000499256.2:p.Asp1699Gly
ENST00000700202.2:c.5096A>G	ENSP00000514856.2:p.Asp1699Gly
ENST00000380152.8:c.5096A>G MANE Select	ENSP00000369497.3:p.Asp1699Gly
ENST00000544455.6:c.5096A>G	ENSP00000439902.1:p.Asp1699Gly
ENST00000614259.2:c.5096A>G	ENSP00000506251.1:p.Asp1699Gly
ENST00000680887.1:c.5096A>G	ENSP00000505508.1:p.Asp1699Gly
ENST00000380152.7:c.5096A>G	ENSP00000369497.3:p.Asp1699Gly
ENST00000544455.5:c.5096A>G	ENSP00000439902.1:p.Asp1699Gly
ENST00000614259.1:n.5096A>G
NM_000059.3:c.5096A>G , LRG_293t1:c.5096A>G	NP_000050.2:p.Asp1699Gly
XM_011535203.1:c.5096A>G	XP_011533505.1:p.Asp1699Gly
XM_011535204.1:c.5096A>G	XP_011533506.1:p.Asp1699Gly
XM_011535205.1:c.5096A>G	XP_011533507.1:p.Asp1699Gly
NM_000059.4:c.5096A>G MANE Select	NP_000050.3:p.Asp1699Gly