Canonical Allele Identifier: CA2082829047

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376737_32376738delinsTG , CM000675.2:g.32376737_32376738delinsTG	GRCh38
NC_000013.10:g.32950874_32950875delinsTG , CM000675.1:g.32950874_32950875delinsTG	GRCh37
NC_000013.9:g.31848874_31848875delinsTG	NCBI36
NG_012772.3:g.66258_66259delinsTG , LRG_293:g.66258_66259delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8700_8701delinsTG	ENSP00000434898.2:p.Asp2900=
ENST00000528762.2:c.*67_*68delinsTG	ENSP00000433168.2:n.*67_*68delinsTG
ENST00000530893.7:c.8331_8332delinsTG	ENSP00000499438.2:p.Asp2777=
ENST00000665585.2:c.*262_*263delinsTG	ENSP00000499570.2:n.*262_*263delinsTG
ENST00000666593.2:c.8700_8701delinsTG	ENSP00000499256.2:p.Asp2900=
ENST00000700202.2:c.8700_8701delinsTG	ENSP00000514856.2:p.Asp2900=
ENST00000700202.1:c.1167_1168delinsTG	ENSP00000514856.1:p.Asp389=
ENST00000700203.1:n.827_828delinsTG
ENST00000380152.8:c.8700_8701delinsTG MANE Select	ENSP00000369497.3:p.Asp2900=
ENST00000544455.6:c.8700_8701delinsTG	ENSP00000439902.1:p.Asp2900=
ENST00000614259.2:c.8708_8709delinsTG	ENSP00000506251.1:n.8708_8709delinsTG
ENST00000665585.1:c.1578_1579delinsTG
ENST00000680887.1:c.8700_8701delinsTG	ENSP00000505508.1:p.Asp2900=
ENST00000380152.7:c.8700_8701delinsTG	ENSP00000369497.3:p.Asp2900=
ENST00000528762.1:c.262_263delinsTG	ENSP00000433168.1:n.262_263delinsTG
ENST00000544455.5:c.8700_8701delinsTG	ENSP00000439902.1:p.Asp2900=
NM_000059.3:c.8700_8701delinsTG , LRG_293t1:c.8700_8701delinsTG	NP_000050.2:p.Asp2900=
XM_011535203.1:c.8700_8701delinsTG	XP_011533505.1:p.Asp2900=
XM_011535204.1:c.8604_8605delinsTG	XP_011533506.1:p.Asp2868=
XM_011535205.1:c.8700_8701delinsTG	XP_011533507.1:p.Asp2900=
NM_000059.4:c.8700_8701delinsTG MANE Select	NP_000050.3:p.Asp2900=