Canonical Allele Identifier: CA2082770431

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32333165_32333166delinsTG , CM000675.2:g.32333165_32333166delinsTG	GRCh38
NC_000013.10:g.32907302_32907303delinsTG , CM000675.1:g.32907302_32907303delinsTG	GRCh37
NC_000013.9:g.31805302_31805303delinsTG	NCBI36
NG_012772.3:g.22686_22687delinsTG , LRG_293:g.22686_22687delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.1687_1688delinsTG	ENSP00000434898.2:p.Trp563=
ENST00000528762.2:c.1687_1688delinsTG	ENSP00000433168.2:p.Trp563=
ENST00000530893.7:c.1318_1319delinsTG	ENSP00000499438.2:p.Trp440=
ENST00000665585.2:c.1687_1688delinsTG	ENSP00000499570.2:p.Trp563=
ENST00000666593.2:c.1687_1688delinsTG	ENSP00000499256.2:p.Trp563=
ENST00000700202.2:c.1687_1688delinsTG	ENSP00000514856.2:p.Trp563=
ENST00000700201.1:c.*1466_*1467delinsTG	ENSP00000514855.1:n.*1466_*1467delinsTG
ENST00000380152.8:c.1687_1688delinsTG MANE Select	ENSP00000369497.3:p.Trp563=
ENST00000544455.6:c.1687_1688delinsTG	ENSP00000439902.1:p.Trp563=
ENST00000614259.2:c.1687_1688delinsTG	ENSP00000506251.1:p.Trp563=
ENST00000680887.1:c.1687_1688delinsTG	ENSP00000505508.1:p.Trp563=
ENST00000380152.7:c.1687_1688delinsTG	ENSP00000369497.3:p.Trp563=
ENST00000530893.6:n.1885_1886delinsTG
ENST00000544455.5:c.1687_1688delinsTG	ENSP00000439902.1:p.Trp563=
ENST00000614259.1:n.1687_1688delinsTG
NM_000059.3:c.1687_1688delinsTG , LRG_293t1:c.1687_1688delinsTG	NP_000050.2:p.Trp563=
XM_011535203.1:c.1687_1688delinsTG	XP_011533505.1:p.Trp563=
XM_011535204.1:c.1687_1688delinsTG	XP_011533506.1:p.Trp563=
XM_011535205.1:c.1687_1688delinsTG	XP_011533507.1:p.Trp563=
NM_000059.4:c.1687_1688delinsTG MANE Select	NP_000050.3:p.Trp563=