Canonical Allele Identifier: CA2082829781

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376821_32376822delinsCT , CM000675.2:g.32376821_32376822delinsCT	GRCh38
NC_000013.10:g.32950958_32950959delinsCT , CM000675.1:g.32950958_32950959delinsCT	GRCh37
NC_000013.9:g.31848958_31848959delinsCT	NCBI36
NG_012772.3:g.66342_66343delinsCT , LRG_293:g.66342_66343delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8754+30_8754+31delinsCT	ENSP00000434898.2:n.8754+30_8754+31delinsCT
ENST00000528762.2:c.*121+30_*121+31delinsCT	ENSP00000433168.2:n.*121+30_*121+31delinsCT
ENST00000530893.7:c.8385+30_8385+31delinsCT	ENSP00000499438.2:n.8385+30_8385+31delinsCT
ENST00000665585.2:c.*316+30_*316+31delinsCT	ENSP00000499570.2:n.*316+30_*316+31delinsCT
ENST00000666593.2:c.8754+30_8754+31delinsCT	ENSP00000499256.2:n.8754+30_8754+31delinsCT
ENST00000700202.2:c.8754+30_8754+31delinsCT	ENSP00000514856.2:n.8754+30_8754+31delinsCT
ENST00000700202.1:c.1221+30_1221+31delinsCT	ENSP00000514856.1:n.1221+30_1221+31delinsCT
ENST00000700203.1:n.881+30_881+31delinsCT
ENST00000380152.8:c.8754+30_8754+31delinsCT MANE Select	ENSP00000369497.3:n.8754+30_8754+31delinsCT
ENST00000544455.6:c.8754+30_8754+31delinsCT	ENSP00000439902.1:n.8754+30_8754+31delinsCT
ENST00000614259.2:c.8762+30_8762+31delinsCT	ENSP00000506251.1:n.8762+30_8762+31delinsCT
ENST00000665585.1:c.1632+30_1632+31delinsCT
ENST00000680887.1:c.8754+30_8754+31delinsCT	ENSP00000505508.1:n.8754+30_8754+31delinsCT
ENST00000380152.7:c.8754+30_8754+31delinsCT	ENSP00000369497.3:n.8754+30_8754+31delinsCT
ENST00000528762.1:c.316+30_316+31delinsCT	ENSP00000433168.1:n.316+30_316+31delinsCT
ENST00000544455.5:c.8754+30_8754+31delinsCT	ENSP00000439902.1:n.8754+30_8754+31delinsCT
NM_000059.3:c.8754+30_8754+31delinsCT , LRG_293t1:c.8754+30_8754+31delinsCT	NP_000050.2:n.8754+30_8754+31delinsCT
XM_011535203.1:c.8754+30_8754+31delinsCT	XP_011533505.1:n.8754+30_8754+31delinsCT
XM_011535204.1:c.8658+30_8658+31delinsCT	XP_011533506.1:n.8658+30_8658+31delinsCT
XM_011535205.1:c.8754+30_8754+31delinsCT	XP_011533507.1:n.8754+30_8754+31delinsCT
NM_000059.4:c.8754+30_8754+31delinsCT MANE Select	NP_000050.3:n.8754+30_8754+31delinsCT