Canonical Allele Identifier: CA2082830926

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362586_32362588delinsCTA , CM000675.2:g.32362586_32362588delinsCTA	GRCh38
NC_000013.10:g.32936723_32936725delinsCTA , CM000675.1:g.32936723_32936725delinsCTA	GRCh37
NC_000013.9:g.31834723_31834725delinsCTA	NCBI36
NG_012772.3:g.52107_52109delinsCTA , LRG_293:g.52107_52109delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7869_7871delinsCTA	ENSP00000434898.2:p.His2623=
ENST00000528762.2:c.7869_7871delinsCTA	ENSP00000433168.2:p.His2623=
ENST00000530893.7:c.7500_7502delinsCTA	ENSP00000499438.2:p.His2500=
ENST00000665585.2:c.7869_7871delinsCTA	ENSP00000499570.2:p.His2623=
ENST00000666593.2:c.7869_7871delinsCTA	ENSP00000499256.2:p.His2623=
ENST00000700202.2:c.7869_7871delinsCTA	ENSP00000514856.2:p.His2623=
ENST00000700202.1:c.336_338delinsCTA	ENSP00000514856.1:p.His112=
ENST00000380152.8:c.7869_7871delinsCTA MANE Select	ENSP00000369497.3:p.His2623=
ENST00000544455.6:c.7869_7871delinsCTA	ENSP00000439902.1:p.His2623=
ENST00000614259.2:c.7877_7879delinsCTA	ENSP00000506251.1:p.Thr2626=
ENST00000665585.1:c.434_436delinsCTA
ENST00000680887.1:c.7869_7871delinsCTA	ENSP00000505508.1:p.His2623=
ENST00000380152.7:c.7869_7871delinsCTA	ENSP00000369497.3:p.His2623=
ENST00000544455.5:c.7869_7871delinsCTA	ENSP00000439902.1:p.His2623=
ENST00000614259.1:n.7877_7879delinsCTA
NM_000059.3:c.7869_7871delinsCTA , LRG_293t1:c.7869_7871delinsCTA	NP_000050.2:p.His2623=
XM_011535203.1:c.7869_7871delinsCTA	XP_011533505.1:p.His2623=
XM_011535204.1:c.7773_7775delinsCTA	XP_011533506.1:p.His2591=
XM_011535205.1:c.7869_7871delinsCTA	XP_011533507.1:p.His2623=
NM_000059.4:c.7869_7871delinsCTA MANE Select	NP_000050.3:p.His2623=