Canonical Allele Identifier: CA2082777726

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32316851_32316859delinsAGGACCCCC , CM000675.2:g.32316851_32316859delinsAGGACCCCC	GRCh38
NC_000013.10:g.32890988_32890996delinsAGGACCCCC , CM000675.1:g.32890988_32890996delinsAGGACCCCC	GRCh37
NC_000013.9:g.31788988_31788996delinsAGGACCCCC	NCBI36
NG_012772.3:g.6372_6380delinsAGGACCCCC , LRG_293:g.6372_6380delinsAGGACCCCC
NG_017006.1:g.96_104delinsGGGGGTCCT
NG_017006.2:g.3505_3513delinsGGGGGTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.67+324_67+332delinsAGGACCCCC	ENSP00000434898.2:n.67+324_67+332delinsAGGACCCCC
ENST00000528762.2:c.67+324_67+332delinsAGGACCCCC	ENSP00000433168.2:n.67+324_67+332delinsAGGACCCCC
ENST00000530893.7:c.-303+328_-303+336delinsAGGACCCCC	ENSP00000499438.2:n.-303+328_-303+336delinsAGGACCCCC
ENST00000665585.2:c.67+324_67+332delinsAGGACCCCC	ENSP00000499570.2:n.67+324_67+332delinsAGGACCCCC
ENST00000666593.2:c.67+324_67+332delinsAGGACCCCC	ENSP00000499256.2:n.67+324_67+332delinsAGGACCCCC
ENST00000700202.2:c.67+324_67+332delinsAGGACCCCC	ENSP00000514856.2:n.67+324_67+332delinsAGGACCCCC
ENST00000700199.1:n.515_523delinsAGGACCCCC
ENST00000700200.1:n.191+324_191+332delinsAGGACCCCC
ENST00000700201.1:c.67+324_67+332delinsAGGACCCCC	ENSP00000514855.1:n.67+324_67+332delinsAGGACCCCC
ENST00000380152.8:c.67+324_67+332delinsAGGACCCCC MANE Select	ENSP00000369497.3:n.67+324_67+332delinsAGGACCCCC
ENST00000544455.6:c.67+324_67+332delinsAGGACCCCC	ENSP00000439902.1:n.67+324_67+332delinsAGGACCCCC
ENST00000614259.2:c.67+324_67+332delinsAGGACCCCC	ENSP00000506251.1:n.67+324_67+332delinsAGGACCCCC
ENST00000680887.1:c.67+324_67+332delinsAGGACCCCC	ENSP00000505508.1:n.67+324_67+332delinsAGGACCCCC
ENST00000380152.7:c.67+324_67+332delinsAGGACCCCC	ENSP00000369497.3:n.67+324_67+332delinsAGGACCCCC
ENST00000530893.6:n.265+328_265+336delinsAGGACCCCC
ENST00000544455.5:c.67+324_67+332delinsAGGACCCCC	ENSP00000439902.1:n.67+324_67+332delinsAGGACCCCC
ENST00000614259.1:n.67+324_67+332delinsAGGACCCCC
NM_000059.3:c.67+324_67+332delinsAGGACCCCC , LRG_293t1:c.67+324_67+332delinsAGGACCCCC	NP_000050.2:n.67+324_67+332delinsAGGACCCCC
XM_011535203.1:c.67+324_67+332delinsAGGACCCCC	XP_011533505.1:n.67+324_67+332delinsAGGACCCCC
XM_011535204.1:c.67+324_67+332delinsAGGACCCCC	XP_011533506.1:n.67+324_67+332delinsAGGACCCCC
XM_011535205.1:c.67+324_67+332delinsAGGACCCCC	XP_011533507.1:n.67+324_67+332delinsAGGACCCCC
NM_000059.4:c.67+324_67+332delinsAGGACCCCC MANE Select	NP_000050.3:n.67+324_67+332delinsAGGACCCCC