Canonical Allele Identifier: CA2082779288

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32317592_32317593delinsTG , CM000675.2:g.32317592_32317593delinsTG	GRCh38
NC_000013.10:g.32891729_32891730delinsTG , CM000675.1:g.32891729_32891730delinsTG	GRCh37
NC_000013.9:g.31789729_31789730delinsTG	NCBI36
NG_012772.3:g.7113_7114delinsTG , LRG_293:g.7113_7114delinsTG
NG_017006.2:g.2771_2772delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.67+1065_67+1066delinsTG	ENSP00000434898.2:n.67+1065_67+1066delinsTG
ENST00000528762.2:c.67+1065_67+1066delinsTG	ENSP00000433168.2:n.67+1065_67+1066delinsTG
ENST00000530893.7:c.-303+1069_-303+1070delinsTG	ENSP00000499438.2:n.-303+1069_-303+1070delinsTG
ENST00000665585.2:c.67+1065_67+1066delinsTG	ENSP00000499570.2:n.67+1065_67+1066delinsTG
ENST00000666593.2:c.67+1065_67+1066delinsTG	ENSP00000499256.2:n.67+1065_67+1066delinsTG
ENST00000700202.2:c.67+1065_67+1066delinsTG	ENSP00000514856.2:n.67+1065_67+1066delinsTG
ENST00000700200.1:n.191+1065_191+1066delinsTG
ENST00000700201.1:c.67+1065_67+1066delinsTG	ENSP00000514855.1:n.67+1065_67+1066delinsTG
ENST00000380152.8:c.67+1065_67+1066delinsTG MANE Select	ENSP00000369497.3:n.67+1065_67+1066delinsTG
ENST00000544455.6:c.67+1065_67+1066delinsTG	ENSP00000439902.1:n.67+1065_67+1066delinsTG
ENST00000614259.2:c.67+1065_67+1066delinsTG	ENSP00000506251.1:n.67+1065_67+1066delinsTG
ENST00000680887.1:c.67+1065_67+1066delinsTG	ENSP00000505508.1:n.67+1065_67+1066delinsTG
ENST00000380152.7:c.67+1065_67+1066delinsTG	ENSP00000369497.3:n.67+1065_67+1066delinsTG
ENST00000530893.6:n.265+1069_265+1070delinsTG
ENST00000544455.5:c.67+1065_67+1066delinsTG	ENSP00000439902.1:n.67+1065_67+1066delinsTG
ENST00000614259.1:n.67+1065_67+1066delinsTG
NM_000059.3:c.67+1065_67+1066delinsTG , LRG_293t1:c.67+1065_67+1066delinsTG	NP_000050.2:n.67+1065_67+1066delinsTG
XM_011535203.1:c.67+1065_67+1066delinsTG	XP_011533505.1:n.67+1065_67+1066delinsTG
XM_011535204.1:c.67+1065_67+1066delinsTG	XP_011533506.1:n.67+1065_67+1066delinsTG
XM_011535205.1:c.67+1065_67+1066delinsTG	XP_011533507.1:n.67+1065_67+1066delinsTG
NM_000059.4:c.67+1065_67+1066delinsTG MANE Select	NP_000050.3:n.67+1065_67+1066delinsTG