Canonical Allele Identifier: CA2082817403

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339294_32339295delinsAC , CM000675.2:g.32339294_32339295delinsAC	GRCh38
NC_000013.10:g.32913431_32913432delinsAC , CM000675.1:g.32913431_32913432delinsAC	GRCh37
NC_000013.9:g.31811431_31811432delinsAC	NCBI36
NG_012772.3:g.28815_28816delinsAC , LRG_293:g.28815_28816delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.4939_4940delinsAC	ENSP00000434898.2:p.Thr1647=
ENST00000528762.2:c.4939_4940delinsAC	ENSP00000433168.2:p.Thr1647=
ENST00000530893.7:c.4570_4571delinsAC	ENSP00000499438.2:p.Thr1524=
ENST00000665585.2:c.4939_4940delinsAC	ENSP00000499570.2:p.Thr1647=
ENST00000666593.2:c.4939_4940delinsAC	ENSP00000499256.2:p.Thr1647=
ENST00000700202.2:c.4939_4940delinsAC	ENSP00000514856.2:p.Thr1647=
ENST00000380152.8:c.4939_4940delinsAC MANE Select	ENSP00000369497.3:p.Thr1647=
ENST00000544455.6:c.4939_4940delinsAC	ENSP00000439902.1:p.Thr1647=
ENST00000614259.2:c.4939_4940delinsAC	ENSP00000506251.1:p.Thr1647=
ENST00000680887.1:c.4939_4940delinsAC	ENSP00000505508.1:p.Thr1647=
ENST00000380152.7:c.4939_4940delinsAC	ENSP00000369497.3:p.Thr1647=
ENST00000544455.5:c.4939_4940delinsAC	ENSP00000439902.1:p.Thr1647=
ENST00000614259.1:n.4939_4940delinsAC
NM_000059.3:c.4939_4940delinsAC , LRG_293t1:c.4939_4940delinsAC	NP_000050.2:p.Thr1647=
XM_011535203.1:c.4939_4940delinsAC	XP_011533505.1:p.Thr1647=
XM_011535204.1:c.4939_4940delinsAC	XP_011533506.1:p.Thr1647=
XM_011535205.1:c.4939_4940delinsAC	XP_011533507.1:p.Thr1647=
NM_000059.4:c.4939_4940delinsAC MANE Select	NP_000050.3:p.Thr1647=