Canonical Allele Identifier: CA2082758915

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32330930C= , CM000675.2:g.32330930C=	GRCh38
NC_000013.10:g.32905067C= , CM000675.1:g.32905067C=	GRCh37
NC_000013.9:g.31803067C=	NCBI36
NG_012772.3:g.20451C= , LRG_293:g.20451C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.693C=	ENSP00000434898.2:p.Ser231=
ENST00000528762.2:c.693C=	ENSP00000433168.2:p.Ser231=
ENST00000530893.7:c.324C=	ENSP00000499438.2:p.Ser108=
ENST00000665585.2:c.693C=	ENSP00000499570.2:p.Ser231=
ENST00000666593.2:c.693C=	ENSP00000499256.2:p.Ser231=
ENST00000700202.2:c.693C=	ENSP00000514856.2:p.Ser231=
ENST00000700201.1:c.*472C=	ENSP00000514855.1:n.*472C=
ENST00000380152.8:c.693C= MANE Select	ENSP00000369497.3:p.Ser231=
ENST00000544455.6:c.693C=	ENSP00000439902.1:p.Ser231=
ENST00000614259.2:c.693C=	ENSP00000506251.1:p.Ser231=
ENST00000680887.1:c.693C=	ENSP00000505508.1:p.Ser231=
ENST00000380152.7:c.693C=	ENSP00000369497.3:p.Ser231=
ENST00000530893.6:n.891C=
ENST00000544455.5:c.693C=	ENSP00000439902.1:p.Ser231=
ENST00000614259.1:n.693C=
NM_000059.3:c.693C= , LRG_293t1:c.693C=	NP_000050.2:p.Ser231=
XM_011535203.1:c.693C=	XP_011533505.1:p.Ser231=
XM_011535204.1:c.693C=	XP_011533506.1:p.Ser231=
XM_011535205.1:c.693C=	XP_011533507.1:p.Ser231=
NM_000059.4:c.693C= MANE Select	NP_000050.3:p.Ser231=