Canonical Allele Identifier: CA2082815971

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371032_32371033delinsTG , CM000675.2:g.32371032_32371033delinsTG	GRCh38
NC_000013.10:g.32945169_32945170delinsTG , CM000675.1:g.32945169_32945170delinsTG	GRCh37
NC_000013.9:g.31843169_31843170delinsTG	NCBI36
NG_012772.3:g.60553_60554delinsTG , LRG_293:g.60553_60554delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8564_8565delinsTG	ENSP00000434898.2:p.Val2855=
ENST00000528762.2:c.8564_8565delinsTG	ENSP00000433168.2:p.Val2855=
ENST00000530893.7:c.8195_8196delinsTG	ENSP00000499438.2:p.Val2732=
ENST00000665585.2:c.8564_8565delinsTG	ENSP00000499570.2:p.Val2855=
ENST00000666593.2:c.8564_8565delinsTG	ENSP00000499256.2:p.Val2855=
ENST00000700202.2:c.8564_8565delinsTG	ENSP00000514856.2:p.Val2855=
ENST00000700202.1:c.1031_1032delinsTG	ENSP00000514856.1:p.Val344=
ENST00000380152.8:c.8564_8565delinsTG MANE Select	ENSP00000369497.3:p.Val2855=
ENST00000544455.6:c.8564_8565delinsTG	ENSP00000439902.1:p.Val2855=
ENST00000614259.2:c.8572_8573delinsTG	ENSP00000506251.1:n.8572_8573delinsTG
ENST00000665585.1:c.1129_1130delinsTG
ENST00000680887.1:c.8564_8565delinsTG	ENSP00000505508.1:p.Val2855=
ENST00000380152.7:c.8564_8565delinsTG	ENSP00000369497.3:p.Val2855=
ENST00000528762.1:c.62_63delinsTG	ENSP00000433168.1:p.Val21=
ENST00000544455.5:c.8564_8565delinsTG	ENSP00000439902.1:p.Val2855=
NM_000059.3:c.8564_8565delinsTG , LRG_293t1:c.8564_8565delinsTG	NP_000050.2:p.Val2855=
XM_011535203.1:c.8564_8565delinsTG	XP_011533505.1:p.Val2855=
XM_011535204.1:c.8468_8469delinsTG	XP_011533506.1:p.Val2823=
XM_011535205.1:c.8564_8565delinsTG	XP_011533507.1:p.Val2855=
NM_000059.4:c.8564_8565delinsTG MANE Select	NP_000050.3:p.Val2855=