Canonical Allele Identifier: CA387766764

Gene: BRCA2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*409A>T	ENSP00000434898.2:n.*409A>T
ENST00000528762.2:c.*1253A>T	ENSP00000433168.2:n.*1253A>T
ENST00000530893.7:c.9517A>T	ENSP00000499438.2:p.Lys3173Ter
ENST00000665585.2:c.*1448A>T	ENSP00000499570.2:n.*1448A>T
ENST00000700202.2:c.9835A>T	ENSP00000514856.2:p.Lys3279Ter
ENST00000700202.1:c.2302A>T	ENSP00000514856.1:p.Lys768Ter
ENST00000700203.1:n.2013A>T
ENST00000380152.8:c.9886A>T MANE Select	ENSP00000369497.3:p.Lys3296Ter
ENST00000544455.6:c.9886A>T	ENSP00000439902.1:p.Lys3296Ter
ENST00000614259.2:c.9894A>T	ENSP00000506251.1:n.9894A>T
ENST00000680887.1:c.9886A>T	ENSP00000505508.1:p.Lys3296Ter
ENST00000380152.7:c.9886A>T	ENSP00000369497.3:p.Lys3296Ter
ENST00000533776.1:n.474A>T
ENST00000544455.5:c.9886A>T	ENSP00000439902.1:p.Lys3296Ter
NM_000059.3:c.9886A>T , LRG_293t1:c.9886A>T	NP_000050.2:p.Lys3296Ter
XM_011535203.1:c.9886A>T	XP_011533505.1:p.Lys3296Ter
XM_011535204.1:c.9790A>T	XP_011533506.1:p.Lys3264Ter
NM_000059.4:c.9886A>T MANE Select	NP_000050.3:p.Lys3296Ter