Canonical Allele Identifier: CA2082834474

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398235C= , CM000675.2:g.32398235C=	GRCh38
NC_000013.10:g.32972372C= , CM000675.1:g.32972372C=	GRCh37
NC_000013.9:g.31870372C=	NCBI36
NG_012772.3:g.87756C= , LRG_293:g.87756C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*245C=	ENSP00000434898.2:n.*245C=
ENST00000528762.2:c.*1089C=	ENSP00000433168.2:n.*1089C=
ENST00000530893.7:c.9353C=	ENSP00000499438.2:p.Ser3118=
ENST00000665585.2:c.*1284C=	ENSP00000499570.2:n.*1284C=
ENST00000700202.2:c.9671C=	ENSP00000514856.2:p.Ser3224=
ENST00000700202.1:c.2138C=	ENSP00000514856.1:p.Ser713=
ENST00000700203.1:n.1849C=
ENST00000380152.8:c.9722C= MANE Select	ENSP00000369497.3:p.Ser3241=
ENST00000544455.6:c.9722C=	ENSP00000439902.1:p.Ser3241=
ENST00000614259.2:c.9730C=	ENSP00000506251.1:n.9730C=
ENST00000680887.1:c.9722C=	ENSP00000505508.1:p.Ser3241=
ENST00000380152.7:c.9722C=	ENSP00000369497.3:p.Ser3241=
ENST00000470094.1:c.805C=
ENST00000533776.1:n.310C=
ENST00000544455.5:c.9722C=	ENSP00000439902.1:p.Ser3241=
NM_000059.3:c.9722C= , LRG_293t1:c.9722C=	NP_000050.2:p.Ser3241=
XM_011535203.1:c.9722C=	XP_011533505.1:p.Ser3241=
XM_011535204.1:c.9626C=	XP_011533506.1:p.Ser3209=
NM_000059.4:c.9722C= MANE Select	NP_000050.3:p.Ser3241=