Canonical Allele Identifier: CA387766774

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664722
• MyVariant Identifiers: chr13:g.32972537A>T (hg19) ; chr13:g.32398400A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398400A>T , CM000675.2:g.32398400A>T	GRCh38
NC_000013.10:g.32972537A>T , CM000675.1:g.32972537A>T	GRCh37
NC_000013.9:g.31870537A>T	NCBI36
NG_012772.3:g.87921A>T , LRG_293:g.87921A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*410A>T	ENSP00000434898.2:n.*410A>T
ENST00000528762.2:c.*1254A>T	ENSP00000433168.2:n.*1254A>T
ENST00000530893.7:c.9518A>T	ENSP00000499438.2:p.Lys3173Met
ENST00000665585.2:c.*1449A>T	ENSP00000499570.2:n.*1449A>T
ENST00000700202.2:c.9836A>T	ENSP00000514856.2:p.Lys3279Met
ENST00000700202.1:c.2303A>T	ENSP00000514856.1:p.Lys768Met
ENST00000700203.1:n.2014A>T
ENST00000380152.8:c.9887A>T MANE Select	ENSP00000369497.3:p.Lys3296Met
ENST00000544455.6:c.9887A>T	ENSP00000439902.1:p.Lys3296Met
ENST00000614259.2:c.9895A>T	ENSP00000506251.1:n.9895A>T
ENST00000680887.1:c.9887A>T	ENSP00000505508.1:p.Lys3296Met
ENST00000380152.7:c.9887A>T	ENSP00000369497.3:p.Lys3296Met
ENST00000533776.1:n.475A>T
ENST00000544455.5:c.9887A>T	ENSP00000439902.1:p.Lys3296Met
NM_000059.3:c.9887A>T , LRG_293t1:c.9887A>T	NP_000050.2:p.Lys3296Met
XM_011535203.1:c.9887A>T	XP_011533505.1:p.Lys3296Met
XM_011535204.1:c.9791A>T	XP_011533506.1:p.Lys3264Met
NM_000059.4:c.9887A>T MANE Select	NP_000050.3:p.Lys3296Met