Canonical Allele Identifier: CA387752874

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32945202T>G (hg19) ; chr13:g.32371065T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371065T>G , CM000675.2:g.32371065T>G	GRCh38
NC_000013.10:g.32945202T>G , CM000675.1:g.32945202T>G	GRCh37
NC_000013.9:g.31843202T>G	NCBI36
NG_012772.3:g.60586T>G , LRG_293:g.60586T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8597T>G	ENSP00000434898.2:p.Phe2866Cys
ENST00000528762.2:c.8597T>G	ENSP00000433168.2:p.Phe2866Cys
ENST00000530893.7:c.8228T>G	ENSP00000499438.2:p.Phe2743Cys
ENST00000665585.2:c.8597T>G	ENSP00000499570.2:p.Phe2866Cys
ENST00000666593.2:c.8597T>G	ENSP00000499256.2:p.Phe2866Cys
ENST00000700202.2:c.8597T>G	ENSP00000514856.2:p.Phe2866Cys
ENST00000700202.1:c.1064T>G	ENSP00000514856.1:p.Phe355Cys
ENST00000380152.8:c.8597T>G MANE Select	ENSP00000369497.3:p.Phe2866Cys
ENST00000544455.6:c.8597T>G	ENSP00000439902.1:p.Phe2866Cys
ENST00000614259.2:c.8605T>G	ENSP00000506251.1:n.8605T>G
ENST00000665585.1:c.1162T>G
ENST00000680887.1:c.8597T>G	ENSP00000505508.1:p.Phe2866Cys
ENST00000380152.7:c.8597T>G	ENSP00000369497.3:p.Phe2866Cys
ENST00000528762.1:c.95T>G	ENSP00000433168.1:p.Phe32Cys
ENST00000544455.5:c.8597T>G	ENSP00000439902.1:p.Phe2866Cys
NM_000059.3:c.8597T>G , LRG_293t1:c.8597T>G	NP_000050.2:p.Phe2866Cys
XM_011535203.1:c.8597T>G	XP_011533505.1:p.Phe2866Cys
XM_011535204.1:c.8501T>G	XP_011533506.1:p.Phe2834Cys
XM_011535205.1:c.8597T>G	XP_011533507.1:p.Phe2866Cys
NM_000059.4:c.8597T>G MANE Select	NP_000050.3:p.Phe2866Cys