Canonical Allele Identifier: CA2082831478

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362628_32362629delinsCT , CM000675.2:g.32362628_32362629delinsCT	GRCh38
NC_000013.10:g.32936765_32936766delinsCT , CM000675.1:g.32936765_32936766delinsCT	GRCh37
NC_000013.9:g.31834765_31834766delinsCT	NCBI36
NG_012772.3:g.52149_52150delinsCT , LRG_293:g.52149_52150delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7911_7912delinsCT	ENSP00000434898.2:p.Ala2637=
ENST00000528762.2:c.7911_7912delinsCT	ENSP00000433168.2:p.Ala2637=
ENST00000530893.7:c.7542_7543delinsCT	ENSP00000499438.2:p.Ala2514=
ENST00000665585.2:c.7911_7912delinsCT	ENSP00000499570.2:p.Ala2637=
ENST00000666593.2:c.7911_7912delinsCT	ENSP00000499256.2:p.Ala2637=
ENST00000700202.2:c.7911_7912delinsCT	ENSP00000514856.2:p.Ala2637=
ENST00000700202.1:c.378_379delinsCT	ENSP00000514856.1:p.Ala126=
ENST00000380152.8:c.7911_7912delinsCT MANE Select	ENSP00000369497.3:p.Ala2637=
ENST00000544455.6:c.7911_7912delinsCT	ENSP00000439902.1:p.Ala2637=
ENST00000614259.2:c.7919_7920delinsCT	ENSP00000506251.1:p.Pro2640=
ENST00000665585.1:c.476_477delinsCT
ENST00000680887.1:c.7911_7912delinsCT	ENSP00000505508.1:p.Ala2637=
ENST00000380152.7:c.7911_7912delinsCT	ENSP00000369497.3:p.Ala2637=
ENST00000544455.5:c.7911_7912delinsCT	ENSP00000439902.1:p.Ala2637=
ENST00000614259.1:n.7919_7920delinsCT
NM_000059.3:c.7911_7912delinsCT , LRG_293t1:c.7911_7912delinsCT	NP_000050.2:p.Ala2637=
XM_011535203.1:c.7911_7912delinsCT	XP_011533505.1:p.Ala2637=
XM_011535204.1:c.7815_7816delinsCT	XP_011533506.1:p.Ala2605=
XM_011535205.1:c.7911_7912delinsCT	XP_011533507.1:p.Ala2637=
NM_000059.4:c.7911_7912delinsCT MANE Select	NP_000050.3:p.Ala2637=