Canonical Allele Identifier: CA2082817306

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357714_32357715delinsCT , CM000675.2:g.32357714_32357715delinsCT	GRCh38
NC_000013.10:g.32931851_32931852delinsCT , CM000675.1:g.32931851_32931852delinsCT	GRCh37
NC_000013.9:g.31829851_31829852delinsCT	NCBI36
NG_012772.3:g.47235_47236delinsCT , LRG_293:g.47235_47236delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7618-28_7618-27delinsCT	ENSP00000434898.2:n.7618-28_7618-27delinsCT
ENST00000528762.2:c.7618-28_7618-27delinsCT	ENSP00000433168.2:n.7618-28_7618-27delinsCT
ENST00000530893.7:c.7249-28_7249-27delinsCT	ENSP00000499438.2:n.7249-28_7249-27delinsCT
ENST00000665585.2:c.7618-28_7618-27delinsCT	ENSP00000499570.2:n.7618-28_7618-27delinsCT
ENST00000666593.2:c.7618-28_7618-27delinsCT	ENSP00000499256.2:n.7618-28_7618-27delinsCT
ENST00000700202.2:c.7618-28_7618-27delinsCT	ENSP00000514856.2:n.7618-28_7618-27delinsCT
ENST00000700202.1:c.85-28_85-27delinsCT	ENSP00000514856.1:n.85-28_85-27delinsCT
ENST00000380152.8:c.7618-28_7618-27delinsCT MANE Select	ENSP00000369497.3:n.7618-28_7618-27delinsCT
ENST00000544455.6:c.7618-28_7618-27delinsCT	ENSP00000439902.1:n.7618-28_7618-27delinsCT
ENST00000614259.2:c.7618-28_7618-27delinsCT	ENSP00000506251.1:n.7618-28_7618-27delinsCT
ENST00000665585.1:c.183-28_183-27delinsCT
ENST00000680887.1:c.7618-28_7618-27delinsCT	ENSP00000505508.1:n.7618-28_7618-27delinsCT
ENST00000380152.7:c.7618-28_7618-27delinsCT	ENSP00000369497.3:n.7618-28_7618-27delinsCT
ENST00000544455.5:c.7618-28_7618-27delinsCT	ENSP00000439902.1:n.7618-28_7618-27delinsCT
ENST00000614259.1:n.7618-28_7618-27delinsCT
NM_000059.3:c.7618-28_7618-27delinsCT , LRG_293t1:c.7618-28_7618-27delinsCT	NP_000050.2:n.7618-28_7618-27delinsCT
XM_011535203.1:c.7618-28_7618-27delinsCT	XP_011533505.1:n.7618-28_7618-27delinsCT
XM_011535204.1:c.7522-28_7522-27delinsCT	XP_011533506.1:n.7522-28_7522-27delinsCT
XM_011535205.1:c.7618-28_7618-27delinsCT	XP_011533507.1:n.7618-28_7618-27delinsCT
NM_000059.4:c.7618-28_7618-27delinsCT MANE Select	NP_000050.3:n.7618-28_7618-27delinsCT