Canonical Allele Identifier: CA2082810929

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32337102_32337103delinsGT , CM000675.2:g.32337102_32337103delinsGT	GRCh38
NC_000013.10:g.32911239_32911240delinsGT , CM000675.1:g.32911239_32911240delinsGT	GRCh37
NC_000013.9:g.31809239_31809240delinsGT	NCBI36
NG_012772.3:g.26623_26624delinsGT , LRG_293:g.26623_26624delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2747_2748delinsGT	ENSP00000434898.2:p.Cys916=
ENST00000528762.2:c.2747_2748delinsGT	ENSP00000433168.2:p.Cys916=
ENST00000530893.7:c.2378_2379delinsGT	ENSP00000499438.2:p.Cys793=
ENST00000665585.2:c.2747_2748delinsGT	ENSP00000499570.2:p.Cys916=
ENST00000666593.2:c.2747_2748delinsGT	ENSP00000499256.2:p.Cys916=
ENST00000700202.2:c.2747_2748delinsGT	ENSP00000514856.2:p.Cys916=
ENST00000380152.8:c.2747_2748delinsGT MANE Select	ENSP00000369497.3:p.Cys916=
ENST00000544455.6:c.2747_2748delinsGT	ENSP00000439902.1:p.Cys916=
ENST00000614259.2:c.2747_2748delinsGT	ENSP00000506251.1:p.Cys916=
ENST00000680887.1:c.2747_2748delinsGT	ENSP00000505508.1:p.Cys916=
ENST00000380152.7:c.2747_2748delinsGT	ENSP00000369497.3:p.Cys916=
ENST00000544455.5:c.2747_2748delinsGT	ENSP00000439902.1:p.Cys916=
ENST00000614259.1:n.2747_2748delinsGT
NM_000059.3:c.2747_2748delinsGT , LRG_293t1:c.2747_2748delinsGT	NP_000050.2:p.Cys916=
XM_011535203.1:c.2747_2748delinsGT	XP_011533505.1:p.Cys916=
XM_011535204.1:c.2747_2748delinsGT	XP_011533506.1:p.Cys916=
XM_011535205.1:c.2747_2748delinsGT	XP_011533507.1:p.Cys916=
NM_000059.4:c.2747_2748delinsGT MANE Select	NP_000050.3:p.Cys916=