Canonical Allele Identifier: CA2018008790

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32356598T= , CM000675.2:g.32356598T=	GRCh38
NC_000013.10:g.32930735T= , CM000675.1:g.32930735T=	GRCh37
NC_000013.9:g.31828735T=	NCBI36
NG_012772.3:g.46119T= , LRG_293:g.46119T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7606T=	ENSP00000434898.2:p.Ser2536=
ENST00000528762.2:c.7606T=	ENSP00000433168.2:p.Ser2536=
ENST00000530893.7:c.7237T=	ENSP00000499438.2:p.Ser2413=
ENST00000665585.2:c.7606T=	ENSP00000499570.2:p.Ser2536=
ENST00000666593.2:c.7606T=	ENSP00000499256.2:p.Ser2536=
ENST00000700202.2:c.7606T=	ENSP00000514856.2:p.Ser2536=
ENST00000700202.1:c.73T=	ENSP00000514856.1:p.Ser25=
ENST00000380152.8:c.7606T= MANE Select	ENSP00000369497.3:p.Ser2536=
ENST00000544455.6:c.7606T=	ENSP00000439902.1:p.Ser2536=
ENST00000614259.2:c.7606T=	ENSP00000506251.1:p.Ser2536=
ENST00000665585.1:c.171T=
ENST00000680887.1:c.7606T=	ENSP00000505508.1:p.Ser2536=
ENST00000380152.7:c.7606T=	ENSP00000369497.3:p.Ser2536=
ENST00000544455.5:c.7606T=	ENSP00000439902.1:p.Ser2536=
ENST00000614259.1:n.7606T=
NM_000059.3:c.7606T= , LRG_293t1:c.7606T=	NP_000050.2:p.Ser2536=
XM_011535203.1:c.7606T=	XP_011533505.1:p.Ser2536=
XM_011535204.1:c.7510T=	XP_011533506.1:p.Ser2504=
XM_011535205.1:c.7606T=	XP_011533507.1:p.Ser2536=
NM_000059.4:c.7606T= MANE Select	NP_000050.3:p.Ser2536=