Canonical Allele Identifier: CA2082811244

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32338737_32338739delinsCCT , CM000675.2:g.32338737_32338739delinsCCT	GRCh38
NC_000013.10:g.32912874_32912876delinsCCT , CM000675.1:g.32912874_32912876delinsCCT	GRCh37
NC_000013.9:g.31810874_31810876delinsCCT	NCBI36
NG_012772.3:g.28258_28260delinsCCT , LRG_293:g.28258_28260delinsCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.4382_4384delinsCCT	ENSP00000434898.2:p.Ser1461=
ENST00000528762.2:c.4382_4384delinsCCT	ENSP00000433168.2:p.Ser1461=
ENST00000530893.7:c.4013_4015delinsCCT	ENSP00000499438.2:p.Ser1338=
ENST00000665585.2:c.4382_4384delinsCCT	ENSP00000499570.2:p.Ser1461=
ENST00000666593.2:c.4382_4384delinsCCT	ENSP00000499256.2:p.Ser1461=
ENST00000700202.2:c.4382_4384delinsCCT	ENSP00000514856.2:p.Ser1461=
ENST00000380152.8:c.4382_4384delinsCCT MANE Select	ENSP00000369497.3:p.Ser1461=
ENST00000544455.6:c.4382_4384delinsCCT	ENSP00000439902.1:p.Ser1461=
ENST00000614259.2:c.4382_4384delinsCCT	ENSP00000506251.1:p.Ser1461=
ENST00000680887.1:c.4382_4384delinsCCT	ENSP00000505508.1:p.Ser1461=
ENST00000380152.7:c.4382_4384delinsCCT	ENSP00000369497.3:p.Ser1461=
ENST00000544455.5:c.4382_4384delinsCCT	ENSP00000439902.1:p.Ser1461=
ENST00000614259.1:n.4382_4384delinsCCT
NM_000059.3:c.4382_4384delinsCCT , LRG_293t1:c.4382_4384delinsCCT	NP_000050.2:p.Ser1461=
XM_011535203.1:c.4382_4384delinsCCT	XP_011533505.1:p.Ser1461=
XM_011535204.1:c.4382_4384delinsCCT	XP_011533506.1:p.Ser1461=
XM_011535205.1:c.4382_4384delinsCCT	XP_011533507.1:p.Ser1461=
NM_000059.4:c.4382_4384delinsCCT MANE Select	NP_000050.3:p.Ser1461=