Canonical Allele Identifier: CA387754814

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 495510
• ClinVar RCV Id: RCV000586864 ; RCV000697605
• dbSNP Id: rs1555288160
• MyVariant Identifiers: chr13:g.32950866T>G (hg19) ; chr13:g.32376729T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376729T>G , CM000675.2:g.32376729T>G	GRCh38
NC_000013.10:g.32950866T>G , CM000675.1:g.32950866T>G	GRCh37
NC_000013.9:g.31848866T>G	NCBI36
NG_012772.3:g.66250T>G , LRG_293:g.66250T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8692T>G	ENSP00000434898.2:p.Leu2898Val
ENST00000528762.2:c.*59T>G	ENSP00000433168.2:n.*59T>G
ENST00000530893.7:c.8323T>G	ENSP00000499438.2:p.Leu2775Val
ENST00000665585.2:c.*254T>G	ENSP00000499570.2:n.*254T>G
ENST00000666593.2:c.8692T>G	ENSP00000499256.2:p.Leu2898Val
ENST00000700202.2:c.8692T>G	ENSP00000514856.2:p.Leu2898Val
ENST00000700202.1:c.1159T>G	ENSP00000514856.1:p.Leu387Val
ENST00000700203.1:n.819T>G
ENST00000380152.8:c.8692T>G MANE Select	ENSP00000369497.3:p.Leu2898Val
ENST00000544455.6:c.8692T>G	ENSP00000439902.1:p.Leu2898Val
ENST00000614259.2:c.8700T>G	ENSP00000506251.1:n.8700T>G
ENST00000665585.1:c.1570T>G
ENST00000680887.1:c.8692T>G	ENSP00000505508.1:p.Leu2898Val
ENST00000380152.7:c.8692T>G	ENSP00000369497.3:p.Leu2898Val
ENST00000528762.1:c.254T>G	ENSP00000433168.1:n.254T>G
ENST00000544455.5:c.8692T>G	ENSP00000439902.1:p.Leu2898Val
NM_000059.3:c.8692T>G , LRG_293t1:c.8692T>G	NP_000050.2:p.Leu2898Val
XM_011535203.1:c.8692T>G	XP_011533505.1:p.Leu2898Val
XM_011535204.1:c.8596T>G	XP_011533506.1:p.Leu2866Val
XM_011535205.1:c.8692T>G	XP_011533507.1:p.Leu2898Val
NM_000059.4:c.8692T>G MANE Select	NP_000050.3:p.Leu2898Val