Canonical Allele Identifier: CA2082776427

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32316528_32316529delinsGT , CM000675.2:g.32316528_32316529delinsGT	GRCh38
NC_000013.10:g.32890665_32890666delinsGT , CM000675.1:g.32890665_32890666delinsGT	GRCh37
NC_000013.9:g.31788665_31788666delinsGT	NCBI36
NG_012772.3:g.6049_6050delinsGT , LRG_293:g.6049_6050delinsGT
NG_017006.1:g.426_427delinsAC
NG_017006.2:g.3835_3836delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.67+1_67+2delinsGT	ENSP00000434898.2:n.67+1_67+2delinsGT
ENST00000528762.2:c.67+1_67+2delinsGT	ENSP00000433168.2:n.67+1_67+2delinsGT
ENST00000530893.7:c.-303+5_-303+6delinsGT	ENSP00000499438.2:n.-303+5_-303+6delinsGT
ENST00000665585.2:c.67+1_67+2delinsGT	ENSP00000499570.2:n.67+1_67+2delinsGT
ENST00000666593.2:c.67+1_67+2delinsGT	ENSP00000499256.2:n.67+1_67+2delinsGT
ENST00000700202.2:c.67+1_67+2delinsGT	ENSP00000514856.2:n.67+1_67+2delinsGT
ENST00000700199.1:n.192_193delinsGT
ENST00000700200.1:n.191+1_191+2delinsGT
ENST00000700201.1:c.67+1_67+2delinsGT	ENSP00000514855.1:n.67+1_67+2delinsGT
ENST00000380152.8:c.67+1_67+2delinsGT MANE Select	ENSP00000369497.3:n.67+1_67+2delinsGT
ENST00000544455.6:c.67+1_67+2delinsGT	ENSP00000439902.1:n.67+1_67+2delinsGT
ENST00000614259.2:c.67+1_67+2delinsGT	ENSP00000506251.1:n.67+1_67+2delinsGT
ENST00000680887.1:c.67+1_67+2delinsGT	ENSP00000505508.1:n.67+1_67+2delinsGT
ENST00000380152.7:c.67+1_67+2delinsGT	ENSP00000369497.3:n.67+1_67+2delinsGT
ENST00000530893.6:n.265+5_265+6delinsGT
ENST00000544455.5:c.67+1_67+2delinsGT	ENSP00000439902.1:n.67+1_67+2delinsGT
ENST00000614259.1:n.67+1_67+2delinsGT
NM_000059.3:c.67+1_67+2delinsGT , LRG_293t1:c.67+1_67+2delinsGT	NP_000050.2:n.67+1_67+2delinsGT
XM_011535203.1:c.67+1_67+2delinsGT	XP_011533505.1:n.67+1_67+2delinsGT
XM_011535204.1:c.67+1_67+2delinsGT	XP_011533506.1:n.67+1_67+2delinsGT
XM_011535205.1:c.67+1_67+2delinsGT	XP_011533507.1:n.67+1_67+2delinsGT
NM_000059.4:c.67+1_67+2delinsGT MANE Select	NP_000050.3:n.67+1_67+2delinsGT