Canonical Allele Identifier: CA2082833347

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362995_32362996delinsTG , CM000675.2:g.32362995_32362996delinsTG	GRCh38
NC_000013.10:g.32937132_32937133delinsTG , CM000675.1:g.32937132_32937133delinsTG	GRCh37
NC_000013.9:g.31835132_31835133delinsTG	NCBI36
NG_012772.3:g.52516_52517delinsTG , LRG_293:g.52516_52517delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7977-184_7977-183delinsTG	ENSP00000434898.2:n.7977-184_7977-183delinsTG
ENST00000528762.2:c.7977-184_7977-183delinsTG	ENSP00000433168.2:n.7977-184_7977-183delinsTG
ENST00000530893.7:c.7608-184_7608-183delinsTG	ENSP00000499438.2:n.7608-184_7608-183delinsTG
ENST00000665585.2:c.7977-184_7977-183delinsTG	ENSP00000499570.2:n.7977-184_7977-183delinsTG
ENST00000666593.2:c.7977-184_7977-183delinsTG	ENSP00000499256.2:n.7977-184_7977-183delinsTG
ENST00000700202.2:c.7977-184_7977-183delinsTG	ENSP00000514856.2:n.7977-184_7977-183delinsTG
ENST00000700202.1:c.444-184_444-183delinsTG	ENSP00000514856.1:n.444-184_444-183delinsTG
ENST00000380152.8:c.7977-184_7977-183delinsTG MANE Select	ENSP00000369497.3:n.7977-184_7977-183delinsTG
ENST00000544455.6:c.7977-184_7977-183delinsTG	ENSP00000439902.1:n.7977-184_7977-183delinsTG
ENST00000614259.2:c.7985-184_7985-183delinsTG	ENSP00000506251.1:n.7985-184_7985-183delinsTG
ENST00000665585.1:c.542-184_542-183delinsTG
ENST00000680887.1:c.7977-184_7977-183delinsTG	ENSP00000505508.1:n.7977-184_7977-183delinsTG
ENST00000380152.7:c.7977-184_7977-183delinsTG	ENSP00000369497.3:n.7977-184_7977-183delinsTG
ENST00000544455.5:c.7977-184_7977-183delinsTG	ENSP00000439902.1:n.7977-184_7977-183delinsTG
NM_000059.3:c.7977-184_7977-183delinsTG , LRG_293t1:c.7977-184_7977-183delinsTG	NP_000050.2:n.7977-184_7977-183delinsTG
XM_011535203.1:c.7977-184_7977-183delinsTG	XP_011533505.1:n.7977-184_7977-183delinsTG
XM_011535204.1:c.7881-184_7881-183delinsTG	XP_011533506.1:n.7881-184_7881-183delinsTG
XM_011535205.1:c.7977-184_7977-183delinsTG	XP_011533507.1:n.7977-184_7977-183delinsTG
NM_000059.4:c.7977-184_7977-183delinsTG MANE Select	NP_000050.3:n.7977-184_7977-183delinsTG