Canonical Allele Identifier: CA387765993

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972438A>C (hg19) ; chr13:g.32398301A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398301A>C , CM000675.2:g.32398301A>C	GRCh38
NC_000013.10:g.32972438A>C , CM000675.1:g.32972438A>C	GRCh37
NC_000013.9:g.31870438A>C	NCBI36
NG_012772.3:g.87822A>C , LRG_293:g.87822A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*311A>C	ENSP00000434898.2:n.*311A>C
ENST00000528762.2:c.*1155A>C	ENSP00000433168.2:n.*1155A>C
ENST00000530893.7:c.9419A>C	ENSP00000499438.2:p.Lys3140Thr
ENST00000665585.2:c.*1350A>C	ENSP00000499570.2:n.*1350A>C
ENST00000700202.2:c.9737A>C	ENSP00000514856.2:p.Lys3246Thr
ENST00000700202.1:c.2204A>C	ENSP00000514856.1:p.Lys735Thr
ENST00000700203.1:n.1915A>C
ENST00000380152.8:c.9788A>C MANE Select	ENSP00000369497.3:p.Lys3263Thr
ENST00000544455.6:c.9788A>C	ENSP00000439902.1:p.Lys3263Thr
ENST00000614259.2:c.9796A>C	ENSP00000506251.1:n.9796A>C
ENST00000680887.1:c.9788A>C	ENSP00000505508.1:p.Lys3263Thr
ENST00000380152.7:c.9788A>C	ENSP00000369497.3:p.Lys3263Thr
ENST00000533776.1:n.376A>C
ENST00000544455.5:c.9788A>C	ENSP00000439902.1:p.Lys3263Thr
NM_000059.3:c.9788A>C , LRG_293t1:c.9788A>C	NP_000050.2:p.Lys3263Thr
XM_011535203.1:c.9788A>C	XP_011533505.1:p.Lys3263Thr
XM_011535204.1:c.9692A>C	XP_011533506.1:p.Lys3231Thr
NM_000059.4:c.9788A>C MANE Select	NP_000050.3:p.Lys3263Thr