Canonical Allele Identifier: CA2082759613

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32331004_32331005delinsCA , CM000675.2:g.32331004_32331005delinsCA	GRCh38
NC_000013.10:g.32905141_32905142delinsCA , CM000675.1:g.32905141_32905142delinsCA	GRCh37
NC_000013.9:g.31803141_31803142delinsCA	NCBI36
NG_012772.3:g.20525_20526delinsCA , LRG_293:g.20525_20526delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.767_768delinsCA	ENSP00000434898.2:p.Thr256=
ENST00000528762.2:c.767_768delinsCA	ENSP00000433168.2:p.Thr256=
ENST00000530893.7:c.398_399delinsCA	ENSP00000499438.2:p.Thr133=
ENST00000665585.2:c.767_768delinsCA	ENSP00000499570.2:p.Thr256=
ENST00000666593.2:c.767_768delinsCA	ENSP00000499256.2:p.Thr256=
ENST00000700202.2:c.767_768delinsCA	ENSP00000514856.2:p.Thr256=
ENST00000700201.1:c.*546_*547delinsCA	ENSP00000514855.1:n.*546_*547delinsCA
ENST00000380152.8:c.767_768delinsCA MANE Select	ENSP00000369497.3:p.Thr256=
ENST00000544455.6:c.767_768delinsCA	ENSP00000439902.1:p.Thr256=
ENST00000614259.2:c.767_768delinsCA	ENSP00000506251.1:p.Thr256=
ENST00000680887.1:c.767_768delinsCA	ENSP00000505508.1:p.Thr256=
ENST00000380152.7:c.767_768delinsCA	ENSP00000369497.3:p.Thr256=
ENST00000530893.6:n.965_966delinsCA
ENST00000544455.5:c.767_768delinsCA	ENSP00000439902.1:p.Thr256=
ENST00000614259.1:n.767_768delinsCA
NM_000059.3:c.767_768delinsCA , LRG_293t1:c.767_768delinsCA	NP_000050.2:p.Thr256=
XM_011535203.1:c.767_768delinsCA	XP_011533505.1:p.Thr256=
XM_011535204.1:c.767_768delinsCA	XP_011533506.1:p.Thr256=
XM_011535205.1:c.767_768delinsCA	XP_011533507.1:p.Thr256=
NM_000059.4:c.767_768delinsCA MANE Select	NP_000050.3:p.Thr256=