Canonical Allele Identifier: CA025605

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52566
• ClinVar RCV Id: RCV000216791 ; RCV000241319 ; RCV000236926 ; RCV000496647 ; RCV003162391
• dbSNP Id: rs397507981
• MyVariant Identifiers: chr13:g.32944571G>A (hg19) ; chr13:g.32370434G>A (hg38)
• PubMed: PMID:22762150

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370434G>A , CM000675.2:g.32370434G>A	GRCh38
NC_000013.10:g.32944571G>A , CM000675.1:g.32944571G>A	GRCh37
NC_000013.9:g.31842571G>A	NCBI36
NG_012772.3:g.59955G>A , LRG_293:g.59955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8364G>A	ENSP00000434898.2:p.Trp2788Ter
ENST00000528762.2:c.8364G>A	ENSP00000433168.2:p.Trp2788Ter
ENST00000530893.7:c.7995G>A	ENSP00000499438.2:p.Trp2665Ter
ENST00000665585.2:c.8364G>A	ENSP00000499570.2:p.Trp2788Ter
ENST00000666593.2:c.8364G>A	ENSP00000499256.2:p.Trp2788Ter
ENST00000700202.2:c.8364G>A	ENSP00000514856.2:p.Trp2788Ter
ENST00000700202.1:c.831G>A	ENSP00000514856.1:p.Trp277Ter
ENST00000380152.8:c.8364G>A MANE Select	ENSP00000369497.3:p.Trp2788Ter
ENST00000544455.6:c.8364G>A	ENSP00000439902.1:p.Trp2788Ter
ENST00000614259.2:c.8372G>A	ENSP00000506251.1:n.8372G>A
ENST00000665585.1:c.929G>A
ENST00000680887.1:c.8364G>A	ENSP00000505508.1:p.Trp2788Ter
ENST00000380152.7:c.8364G>A	ENSP00000369497.3:p.Trp2788Ter
ENST00000544455.5:c.8364G>A	ENSP00000439902.1:p.Trp2788Ter
NM_000059.3:c.8364G>A , LRG_293t1:c.8364G>A	NP_000050.2:p.Trp2788Ter
XM_011535203.1:c.8364G>A	XP_011533505.1:p.Trp2788Ter
XM_011535204.1:c.8268G>A	XP_011533506.1:p.Trp2756Ter
XM_011535205.1:c.8364G>A	XP_011533507.1:p.Trp2788Ter
NM_000059.4:c.8364G>A MANE Select	NP_000050.3:p.Trp2788Ter