Canonical Allele Identifier: CA2082784359

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319296_32319302delinsAAGAATT , CM000675.2:g.32319296_32319302delinsAAGAATT	GRCh38
NC_000013.10:g.32893433_32893439delinsAAGAATT , CM000675.1:g.32893433_32893439delinsAAGAATT	GRCh37
NC_000013.9:g.31791433_31791439delinsAAGAATT	NCBI36
NG_012772.3:g.8817_8823delinsAAGAATT , LRG_293:g.8817_8823delinsAAGAATT
NG_017006.2:g.1062_1068delinsAATTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.287_293delinsAAGAATT	ENSP00000434898.2:p.Lys96=
ENST00000528762.2:c.287_293delinsAAGAATT	ENSP00000433168.2:p.Lys96=
ENST00000530893.7:c.-83_-77delinsAAGAATT	ENSP00000499438.2:n.-83_-77delinsAAGAATT
ENST00000665585.2:c.287_293delinsAAGAATT	ENSP00000499570.2:p.Lys96=
ENST00000666593.2:c.287_293delinsAAGAATT	ENSP00000499256.2:p.Lys96=
ENST00000700202.2:c.287_293delinsAAGAATT	ENSP00000514856.2:p.Lys96=
ENST00000700200.1:n.191+2769_191+2775delinsAAGAATT
ENST00000700201.1:c.287_293delinsAAGAATT	ENSP00000514855.1:p.Lys96=
ENST00000380152.8:c.287_293delinsAAGAATT MANE Select	ENSP00000369497.3:p.Lys96=
ENST00000544455.6:c.287_293delinsAAGAATT	ENSP00000439902.1:p.Lys96=
ENST00000614259.2:c.287_293delinsAAGAATT	ENSP00000506251.1:p.Lys96=
ENST00000680887.1:c.287_293delinsAAGAATT	ENSP00000505508.1:p.Lys96=
ENST00000380152.7:c.287_293delinsAAGAATT	ENSP00000369497.3:p.Lys96=
ENST00000530893.6:n.485_491delinsAAGAATT
ENST00000544455.5:c.287_293delinsAAGAATT	ENSP00000439902.1:p.Lys96=
ENST00000614259.1:n.287_293delinsAAGAATT
NM_000059.3:c.287_293delinsAAGAATT , LRG_293t1:c.287_293delinsAAGAATT	NP_000050.2:p.Lys96=
XM_011535203.1:c.287_293delinsAAGAATT	XP_011533505.1:p.Lys96=
XM_011535204.1:c.287_293delinsAAGAATT	XP_011533506.1:p.Lys96=
XM_011535205.1:c.287_293delinsAAGAATT	XP_011533507.1:p.Lys96=
NM_000059.4:c.287_293delinsAAGAATT MANE Select	NP_000050.3:p.Lys96=