Canonical Allele Identifier: CA387766763

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664707
• MyVariant Identifiers: chr13:g.32972536A>G (hg19) ; chr13:g.32398399A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398399A>G , CM000675.2:g.32398399A>G	GRCh38
NC_000013.10:g.32972536A>G , CM000675.1:g.32972536A>G	GRCh37
NC_000013.9:g.31870536A>G	NCBI36
NG_012772.3:g.87920A>G , LRG_293:g.87920A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*409A>G	ENSP00000434898.2:n.*409A>G
ENST00000528762.2:c.*1253A>G	ENSP00000433168.2:n.*1253A>G
ENST00000530893.7:c.9517A>G	ENSP00000499438.2:p.Lys3173Glu
ENST00000665585.2:c.*1448A>G	ENSP00000499570.2:n.*1448A>G
ENST00000700202.2:c.9835A>G	ENSP00000514856.2:p.Lys3279Glu
ENST00000700202.1:c.2302A>G	ENSP00000514856.1:p.Lys768Glu
ENST00000700203.1:n.2013A>G
ENST00000380152.8:c.9886A>G MANE Select	ENSP00000369497.3:p.Lys3296Glu
ENST00000544455.6:c.9886A>G	ENSP00000439902.1:p.Lys3296Glu
ENST00000614259.2:c.9894A>G	ENSP00000506251.1:n.9894A>G
ENST00000680887.1:c.9886A>G	ENSP00000505508.1:p.Lys3296Glu
ENST00000380152.7:c.9886A>G	ENSP00000369497.3:p.Lys3296Glu
ENST00000533776.1:n.474A>G
ENST00000544455.5:c.9886A>G	ENSP00000439902.1:p.Lys3296Glu
NM_000059.3:c.9886A>G , LRG_293t1:c.9886A>G	NP_000050.2:p.Lys3296Glu
XM_011535203.1:c.9886A>G	XP_011533505.1:p.Lys3296Glu
XM_011535204.1:c.9790A>G	XP_011533506.1:p.Lys3264Glu
NM_000059.4:c.9886A>G MANE Select	NP_000050.3:p.Lys3296Glu