Canonical Allele Identifier: CA2082813347

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370437T= , CM000675.2:g.32370437T=	GRCh38
NC_000013.10:g.32944574T= , CM000675.1:g.32944574T=	GRCh37
NC_000013.9:g.31842574T=	NCBI36
NG_012772.3:g.59958T= , LRG_293:g.59958T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8367T=	ENSP00000434898.2:p.Tyr2789=
ENST00000528762.2:c.8367T=	ENSP00000433168.2:p.Tyr2789=
ENST00000530893.7:c.7998T=	ENSP00000499438.2:p.Tyr2666=
ENST00000665585.2:c.8367T=	ENSP00000499570.2:p.Tyr2789=
ENST00000666593.2:c.8367T=	ENSP00000499256.2:p.Tyr2789=
ENST00000700202.2:c.8367T=	ENSP00000514856.2:p.Tyr2789=
ENST00000700202.1:c.834T=	ENSP00000514856.1:p.Tyr278=
ENST00000380152.8:c.8367T= MANE Select	ENSP00000369497.3:p.Tyr2789=
ENST00000544455.6:c.8367T=	ENSP00000439902.1:p.Tyr2789=
ENST00000614259.2:c.8375T=	ENSP00000506251.1:n.8375T=
ENST00000665585.1:c.932T=
ENST00000680887.1:c.8367T=	ENSP00000505508.1:p.Tyr2789=
ENST00000380152.7:c.8367T=	ENSP00000369497.3:p.Tyr2789=
ENST00000544455.5:c.8367T=	ENSP00000439902.1:p.Tyr2789=
NM_000059.3:c.8367T= , LRG_293t1:c.8367T=	NP_000050.2:p.Tyr2789=
XM_011535203.1:c.8367T=	XP_011533505.1:p.Tyr2789=
XM_011535204.1:c.8271T=	XP_011533506.1:p.Tyr2757=
XM_011535205.1:c.8367T=	XP_011533507.1:p.Tyr2789=
NM_000059.4:c.8367T= MANE Select	NP_000050.3:p.Tyr2789=