Canonical Allele Identifier: CA2082782829

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319131C= , CM000675.2:g.32319131C=	GRCh38
NC_000013.10:g.32893268C= , CM000675.1:g.32893268C=	GRCh37
NC_000013.9:g.31791268C=	NCBI36
NG_012772.3:g.8652C= , LRG_293:g.8652C=
NG_017006.2:g.1233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.122C=	ENSP00000434898.2:p.Pro41=
ENST00000528762.2:c.122C=	ENSP00000433168.2:p.Pro41=
ENST00000530893.7:c.-248C=	ENSP00000499438.2:n.-248C=
ENST00000665585.2:c.122C=	ENSP00000499570.2:p.Pro41=
ENST00000666593.2:c.122C=	ENSP00000499256.2:p.Pro41=
ENST00000700202.2:c.122C=	ENSP00000514856.2:p.Pro41=
ENST00000700200.1:n.191+2604C=
ENST00000700201.1:c.122C=	ENSP00000514855.1:p.Pro41=
ENST00000380152.8:c.122C= MANE Select	ENSP00000369497.3:p.Pro41=
ENST00000544455.6:c.122C=	ENSP00000439902.1:p.Pro41=
ENST00000614259.2:c.122C=	ENSP00000506251.1:p.Pro41=
ENST00000680887.1:c.122C=	ENSP00000505508.1:p.Pro41=
ENST00000380152.7:c.122C=	ENSP00000369497.3:p.Pro41=
ENST00000530893.6:n.320C=
ENST00000544455.5:c.122C=	ENSP00000439902.1:p.Pro41=
ENST00000614259.1:n.122C=
NM_000059.3:c.122C= , LRG_293t1:c.122C=	NP_000050.2:p.Pro41=
XM_011535203.1:c.122C=	XP_011533505.1:p.Pro41=
XM_011535204.1:c.122C=	XP_011533506.1:p.Pro41=
XM_011535205.1:c.122C=	XP_011533507.1:p.Pro41=
NM_000059.4:c.122C= MANE Select	NP_000050.3:p.Pro41=