Canonical Allele Identifier: CA2082816504

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371086T= , CM000675.2:g.32371086T=	GRCh38
NC_000013.10:g.32945223T= , CM000675.1:g.32945223T=	GRCh37
NC_000013.9:g.31843223T=	NCBI36
NG_012772.3:g.60607T= , LRG_293:g.60607T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8618T=	ENSP00000434898.2:p.Phe2873=
ENST00000528762.2:c.8618T=	ENSP00000433168.2:p.Phe2873=
ENST00000530893.7:c.8249T=	ENSP00000499438.2:p.Phe2750=
ENST00000665585.2:c.8618T=	ENSP00000499570.2:p.Phe2873=
ENST00000666593.2:c.8618T=	ENSP00000499256.2:p.Phe2873=
ENST00000700202.2:c.8618T=	ENSP00000514856.2:p.Phe2873=
ENST00000700202.1:c.1085T=	ENSP00000514856.1:p.Phe362=
ENST00000380152.8:c.8618T= MANE Select	ENSP00000369497.3:p.Phe2873=
ENST00000544455.6:c.8618T=	ENSP00000439902.1:p.Phe2873=
ENST00000614259.2:c.8626T=	ENSP00000506251.1:n.8626T=
ENST00000665585.1:c.1183T=
ENST00000680887.1:c.8618T=	ENSP00000505508.1:p.Phe2873=
ENST00000380152.7:c.8618T=	ENSP00000369497.3:p.Phe2873=
ENST00000528762.1:c.116T=	ENSP00000433168.1:p.Phe39=
ENST00000544455.5:c.8618T=	ENSP00000439902.1:p.Phe2873=
NM_000059.3:c.8618T= , LRG_293t1:c.8618T=	NP_000050.2:p.Phe2873=
XM_011535203.1:c.8618T=	XP_011533505.1:p.Phe2873=
XM_011535204.1:c.8522T=	XP_011533506.1:p.Phe2841=
XM_011535205.1:c.8618T=	XP_011533507.1:p.Phe2873=
NM_000059.4:c.8618T= MANE Select	NP_000050.3:p.Phe2873=