Canonical Allele Identifier: CA2082832359

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362695_32362697delinsCAA , CM000675.2:g.32362695_32362697delinsCAA	GRCh38
NC_000013.10:g.32936832_32936834delinsCAA , CM000675.1:g.32936832_32936834delinsCAA	GRCh37
NC_000013.9:g.31834832_31834834delinsCAA	NCBI36
NG_012772.3:g.52216_52218delinsCAA , LRG_293:g.52216_52218delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7976+2_7976+4delinsCAA	ENSP00000434898.2:n.7976+2_7976+4delinsCAA
ENST00000528762.2:c.7976+2_7976+4delinsCAA	ENSP00000433168.2:n.7976+2_7976+4delinsCAA
ENST00000530893.7:c.7607+2_7607+4delinsCAA	ENSP00000499438.2:n.7607+2_7607+4delinsCAA
ENST00000665585.2:c.7976+2_7976+4delinsCAA	ENSP00000499570.2:n.7976+2_7976+4delinsCAA
ENST00000666593.2:c.7976+2_7976+4delinsCAA	ENSP00000499256.2:n.7976+2_7976+4delinsCAA
ENST00000700202.2:c.7976+2_7976+4delinsCAA	ENSP00000514856.2:n.7976+2_7976+4delinsCAA
ENST00000700202.1:c.443+2_443+4delinsCAA	ENSP00000514856.1:n.443+2_443+4delinsCAA
ENST00000380152.8:c.7976+2_7976+4delinsCAA MANE Select	ENSP00000369497.3:n.7976+2_7976+4delinsCAA
ENST00000544455.6:c.7976+2_7976+4delinsCAA	ENSP00000439902.1:n.7976+2_7976+4delinsCAA
ENST00000614259.2:c.7984+2_7984+4delinsCAA	ENSP00000506251.1:n.7984+2_7984+4delinsCAA
ENST00000665585.1:c.541+2_541+4delinsCAA
ENST00000680887.1:c.7976+2_7976+4delinsCAA	ENSP00000505508.1:n.7976+2_7976+4delinsCAA
ENST00000380152.7:c.7976+2_7976+4delinsCAA	ENSP00000369497.3:n.7976+2_7976+4delinsCAA
ENST00000544455.5:c.7976+2_7976+4delinsCAA	ENSP00000439902.1:n.7976+2_7976+4delinsCAA
NM_000059.3:c.7976+2_7976+4delinsCAA , LRG_293t1:c.7976+2_7976+4delinsCAA	NP_000050.2:n.7976+2_7976+4delinsCAA
XM_011535203.1:c.7976+2_7976+4delinsCAA	XP_011533505.1:n.7976+2_7976+4delinsCAA
XM_011535204.1:c.7880+2_7880+4delinsCAA	XP_011533506.1:n.7880+2_7880+4delinsCAA
XM_011535205.1:c.7976+2_7976+4delinsCAA	XP_011533507.1:n.7976+2_7976+4delinsCAA
NM_000059.4:c.7976+2_7976+4delinsCAA MANE Select	NP_000050.3:n.7976+2_7976+4delinsCAA