Canonical Allele Identifier: CA2082831455

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362626_32362631delinsGCCTTT , CM000675.2:g.32362626_32362631delinsGCCTTT	GRCh38
NC_000013.10:g.32936763_32936768delinsGCCTTT , CM000675.1:g.32936763_32936768delinsGCCTTT	GRCh37
NC_000013.9:g.31834763_31834768delinsGCCTTT	NCBI36
NG_012772.3:g.52147_52152delinsGCCTTT , LRG_293:g.52147_52152delinsGCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7909_7914delinsGCCTTT	ENSP00000434898.2:p.Ala2637=
ENST00000528762.2:c.7909_7914delinsGCCTTT	ENSP00000433168.2:p.Ala2637=
ENST00000530893.7:c.7540_7545delinsGCCTTT	ENSP00000499438.2:p.Ala2514=
ENST00000665585.2:c.7909_7914delinsGCCTTT	ENSP00000499570.2:p.Ala2637=
ENST00000666593.2:c.7909_7914delinsGCCTTT	ENSP00000499256.2:p.Ala2637=
ENST00000700202.2:c.7909_7914delinsGCCTTT	ENSP00000514856.2:p.Ala2637=
ENST00000700202.1:c.376_381delinsGCCTTT	ENSP00000514856.1:p.Ala126=
ENST00000380152.8:c.7909_7914delinsGCCTTT MANE Select	ENSP00000369497.3:p.Ala2637=
ENST00000544455.6:c.7909_7914delinsGCCTTT	ENSP00000439902.1:p.Ala2637=
ENST00000614259.2:c.7917_7922delinsGCCTTT	ENSP00000506251.1:p.Val2639=
ENST00000665585.1:c.474_479delinsGCCTTT
ENST00000680887.1:c.7909_7914delinsGCCTTT	ENSP00000505508.1:p.Ala2637=
ENST00000380152.7:c.7909_7914delinsGCCTTT	ENSP00000369497.3:p.Ala2637=
ENST00000544455.5:c.7909_7914delinsGCCTTT	ENSP00000439902.1:p.Ala2637=
ENST00000614259.1:n.7917_7922delinsGCCTTT
NM_000059.3:c.7909_7914delinsGCCTTT , LRG_293t1:c.7909_7914delinsGCCTTT	NP_000050.2:p.Ala2637=
XM_011535203.1:c.7909_7914delinsGCCTTT	XP_011533505.1:p.Ala2637=
XM_011535204.1:c.7813_7818delinsGCCTTT	XP_011533506.1:p.Ala2605=
XM_011535205.1:c.7909_7914delinsGCCTTT	XP_011533507.1:p.Ala2637=
NM_000059.4:c.7909_7914delinsGCCTTT MANE Select	NP_000050.3:p.Ala2637=