Canonical Allele Identifier: CA2082784689

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319335_32319364delinsGCAATATGGTAGACTGGGGAGAACTACAAA , CM000675.2:g.32319335_32319364delinsGCAATATGGTAGACTGGGGAGAACTACAAA	GRCh38
NC_000013.10:g.32893472_32893501delinsGCAATATGGTAGACTGGGGAGAACTACAAA , CM000675.1:g.32893472_32893501delinsGCAATATGGTAGACTGGGGAGAACTACAAA	GRCh37
NC_000013.9:g.31791472_31791501delinsGCAATATGGTAGACTGGGGAGAACTACAAA	NCBI36
NG_012772.3:g.8856_8885delinsGCAATATGGTAGACTGGGGAGAACTACAAA , LRG_293:g.8856_8885delinsGCAATATGGTAGACTGGGGAGAACTACAAA
NG_017006.2:g.1000_1029delinsTTTGTAGTTCTCCCCAGTCTACCATATTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000434898.2:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000528762.2:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000433168.2:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000530893.7:c.-54+10_-54+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000499438.2:n.-54+10_-54+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000665585.2:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000499570.2:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000666593.2:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000499256.2:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000700202.2:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000514856.2:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000700200.1:n.191+2808_191+2837delinsGCAATATGGTAGACTGGGGAGAACTACAAA
ENST00000700201.1:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000514855.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000380152.8:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA MANE Select	ENSP00000369497.3:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000544455.6:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000439902.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000614259.2:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000506251.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000680887.1:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000505508.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000380152.7:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000369497.3:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000530893.6:n.514+10_514+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA
ENST00000544455.5:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	ENSP00000439902.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGA...
ENST00000614259.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA
NM_000059.3:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA , LRG_293t1:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	NP_000050.2:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACA...
XM_011535203.1:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	XP_011533505.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACT...
XM_011535204.1:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	XP_011533506.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACT...
XM_011535205.1:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA	XP_011533507.1:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACT...
NM_000059.4:c.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACAAA MANE Select	NP_000050.3:n.316+10_316+39delinsGCAATATGGTAGACTGGGGAGAACTACA...