Canonical Allele Identifier: CA2082817183

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357629_32357630delinsGT , CM000675.2:g.32357629_32357630delinsGT	GRCh38
NC_000013.10:g.32931766_32931767delinsGT , CM000675.1:g.32931766_32931767delinsGT	GRCh37
NC_000013.9:g.31829766_31829767delinsGT	NCBI36
NG_012772.3:g.47150_47151delinsGT , LRG_293:g.47150_47151delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7618-113_7618-112delinsGT	ENSP00000434898.2:n.7618-113_7618-112delinsGT
ENST00000528762.2:c.7618-113_7618-112delinsGT	ENSP00000433168.2:n.7618-113_7618-112delinsGT
ENST00000530893.7:c.7249-113_7249-112delinsGT	ENSP00000499438.2:n.7249-113_7249-112delinsGT
ENST00000665585.2:c.7618-113_7618-112delinsGT	ENSP00000499570.2:n.7618-113_7618-112delinsGT
ENST00000666593.2:c.7618-113_7618-112delinsGT	ENSP00000499256.2:n.7618-113_7618-112delinsGT
ENST00000700202.2:c.7618-113_7618-112delinsGT	ENSP00000514856.2:n.7618-113_7618-112delinsGT
ENST00000700202.1:c.85-113_85-112delinsGT	ENSP00000514856.1:n.85-113_85-112delinsGT
ENST00000380152.8:c.7618-113_7618-112delinsGT MANE Select	ENSP00000369497.3:n.7618-113_7618-112delinsGT
ENST00000544455.6:c.7618-113_7618-112delinsGT	ENSP00000439902.1:n.7618-113_7618-112delinsGT
ENST00000614259.2:c.7618-113_7618-112delinsGT	ENSP00000506251.1:n.7618-113_7618-112delinsGT
ENST00000665585.1:c.183-113_183-112delinsGT
ENST00000680887.1:c.7618-113_7618-112delinsGT	ENSP00000505508.1:n.7618-113_7618-112delinsGT
ENST00000380152.7:c.7618-113_7618-112delinsGT	ENSP00000369497.3:n.7618-113_7618-112delinsGT
ENST00000544455.5:c.7618-113_7618-112delinsGT	ENSP00000439902.1:n.7618-113_7618-112delinsGT
ENST00000614259.1:n.7618-113_7618-112delinsGT
NM_000059.3:c.7618-113_7618-112delinsGT , LRG_293t1:c.7618-113_7618-112delinsGT	NP_000050.2:n.7618-113_7618-112delinsGT
XM_011535203.1:c.7618-113_7618-112delinsGT	XP_011533505.1:n.7618-113_7618-112delinsGT
XM_011535204.1:c.7522-113_7522-112delinsGT	XP_011533506.1:n.7522-113_7522-112delinsGT
XM_011535205.1:c.7618-113_7618-112delinsGT	XP_011533507.1:n.7618-113_7618-112delinsGT
NM_000059.4:c.7618-113_7618-112delinsGT MANE Select	NP_000050.3:n.7618-113_7618-112delinsGT