Canonical Allele Identifier: CA2082837309

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379741_32379745delinsTCCAA , CM000675.2:g.32379741_32379745delinsTCCAA	GRCh38
NC_000013.10:g.32953878_32953882delinsTCCAA , CM000675.1:g.32953878_32953882delinsTCCAA	GRCh37
NC_000013.9:g.31851878_31851882delinsTCCAA	NCBI36
NG_012772.3:g.69262_69266delinsTCCAA , LRG_293:g.69262_69266delinsTCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8954-9_8954-5delinsTCCAA	ENSP00000434898.2:n.8954-9_8954-5delinsTCCAA
ENST00000528762.2:c.*321-9_*321-5delinsTCCAA	ENSP00000433168.2:n.*321-9_*321-5delinsTCCAA
ENST00000530893.7:c.8585-9_8585-5delinsTCCAA	ENSP00000499438.2:n.8585-9_8585-5delinsTCCAA
ENST00000665585.2:c.*516-9_*516-5delinsTCCAA	ENSP00000499570.2:n.*516-9_*516-5delinsTCCAA
ENST00000666593.2:c.8954-9_8954-5delinsTCCAA	ENSP00000499256.2:n.8954-9_8954-5delinsTCCAA
ENST00000700202.2:c.8954-60_8954-56delinsTCCAA	ENSP00000514856.2:n.8954-60_8954-56delinsTCCAA
ENST00000700202.1:c.1421-60_1421-56delinsTCCAA	ENSP00000514856.1:n.1421-60_1421-56delinsTCCAA
ENST00000700203.1:n.1081-9_1081-5delinsTCCAA
ENST00000380152.8:c.8954-9_8954-5delinsTCCAA MANE Select	ENSP00000369497.3:n.8954-9_8954-5delinsTCCAA
ENST00000544455.6:c.8954-9_8954-5delinsTCCAA	ENSP00000439902.1:n.8954-9_8954-5delinsTCCAA
ENST00000614259.2:c.8962-9_8962-5delinsTCCAA	ENSP00000506251.1:n.8962-9_8962-5delinsTCCAA
ENST00000665585.1:c.1832-9_1832-5delinsTCCAA
ENST00000680887.1:c.8954-9_8954-5delinsTCCAA	ENSP00000505508.1:n.8954-9_8954-5delinsTCCAA
ENST00000380152.7:c.8954-9_8954-5delinsTCCAA	ENSP00000369497.3:n.8954-9_8954-5delinsTCCAA
ENST00000544455.5:c.8954-9_8954-5delinsTCCAA	ENSP00000439902.1:n.8954-9_8954-5delinsTCCAA
NM_000059.3:c.8954-9_8954-5delinsTCCAA , LRG_293t1:c.8954-9_8954-5delinsTCCAA	NP_000050.2:n.8954-9_8954-5delinsTCCAA
XM_011535203.1:c.8954-9_8954-5delinsTCCAA	XP_011533505.1:n.8954-9_8954-5delinsTCCAA
XM_011535204.1:c.8858-9_8858-5delinsTCCAA	XP_011533506.1:n.8858-9_8858-5delinsTCCAA
XM_011535205.1:c.8755-9_8755-5delinsTCCAA	XP_011533507.1:n.8755-9_8755-5delinsTCCAA
NM_000059.4:c.8954-9_8954-5delinsTCCAA MANE Select	NP_000050.3:n.8954-9_8954-5delinsTCCAA