Canonical Allele Identifier: CA2082833489

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363064_32363068delinsCTCAG , CM000675.2:g.32363064_32363068delinsCTCAG	GRCh38
NC_000013.10:g.32937201_32937205delinsCTCAG , CM000675.1:g.32937201_32937205delinsCTCAG	GRCh37
NC_000013.9:g.31835201_31835205delinsCTCAG	NCBI36
NG_012772.3:g.52585_52589delinsCTCAG , LRG_293:g.52585_52589delinsCTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7977-115_7977-111delinsCTCAG	ENSP00000434898.2:n.7977-115_7977-111delinsCTCAG
ENST00000528762.2:c.7977-115_7977-111delinsCTCAG	ENSP00000433168.2:n.7977-115_7977-111delinsCTCAG
ENST00000530893.7:c.7608-115_7608-111delinsCTCAG	ENSP00000499438.2:n.7608-115_7608-111delinsCTCAG
ENST00000665585.2:c.7977-115_7977-111delinsCTCAG	ENSP00000499570.2:n.7977-115_7977-111delinsCTCAG
ENST00000666593.2:c.7977-115_7977-111delinsCTCAG	ENSP00000499256.2:n.7977-115_7977-111delinsCTCAG
ENST00000700202.2:c.7977-115_7977-111delinsCTCAG	ENSP00000514856.2:n.7977-115_7977-111delinsCTCAG
ENST00000700202.1:c.444-115_444-111delinsCTCAG	ENSP00000514856.1:n.444-115_444-111delinsCTCAG
ENST00000380152.8:c.7977-115_7977-111delinsCTCAG MANE Select	ENSP00000369497.3:n.7977-115_7977-111delinsCTCAG
ENST00000544455.6:c.7977-115_7977-111delinsCTCAG	ENSP00000439902.1:n.7977-115_7977-111delinsCTCAG
ENST00000614259.2:c.7985-115_7985-111delinsCTCAG	ENSP00000506251.1:n.7985-115_7985-111delinsCTCAG
ENST00000665585.1:c.542-115_542-111delinsCTCAG
ENST00000680887.1:c.7977-115_7977-111delinsCTCAG	ENSP00000505508.1:n.7977-115_7977-111delinsCTCAG
ENST00000380152.7:c.7977-115_7977-111delinsCTCAG	ENSP00000369497.3:n.7977-115_7977-111delinsCTCAG
ENST00000544455.5:c.7977-115_7977-111delinsCTCAG	ENSP00000439902.1:n.7977-115_7977-111delinsCTCAG
NM_000059.3:c.7977-115_7977-111delinsCTCAG , LRG_293t1:c.7977-115_7977-111delinsCTCAG	NP_000050.2:n.7977-115_7977-111delinsCTCAG
XM_011535203.1:c.7977-115_7977-111delinsCTCAG	XP_011533505.1:n.7977-115_7977-111delinsCTCAG
XM_011535204.1:c.7881-115_7881-111delinsCTCAG	XP_011533506.1:n.7881-115_7881-111delinsCTCAG
XM_011535205.1:c.7977-115_7977-111delinsCTCAG	XP_011533507.1:n.7977-115_7977-111delinsCTCAG
NM_000059.4:c.7977-115_7977-111delinsCTCAG MANE Select	NP_000050.3:n.7977-115_7977-111delinsCTCAG