Canonical Allele Identifier: CA2082781732

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32318879_32318881delinsCTT , CM000675.2:g.32318879_32318881delinsCTT	GRCh38
NC_000013.10:g.32893016_32893018delinsCTT , CM000675.1:g.32893016_32893018delinsCTT	GRCh37
NC_000013.9:g.31791016_31791018delinsCTT	NCBI36
NG_012772.3:g.8400_8402delinsCTT , LRG_293:g.8400_8402delinsCTT
NG_017006.2:g.1483_1485delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.68-198_68-196delinsCTT	ENSP00000434898.2:n.68-198_68-196delinsCTT
ENST00000528762.2:c.68-198_68-196delinsCTT	ENSP00000433168.2:n.68-198_68-196delinsCTT
ENST00000530893.7:c.-302-198_-302-196delinsCTT	ENSP00000499438.2:n.-302-198_-302-196delinsCTT
ENST00000665585.2:c.68-198_68-196delinsCTT	ENSP00000499570.2:n.68-198_68-196delinsCTT
ENST00000666593.2:c.68-198_68-196delinsCTT	ENSP00000499256.2:n.68-198_68-196delinsCTT
ENST00000700202.2:c.68-198_68-196delinsCTT	ENSP00000514856.2:n.68-198_68-196delinsCTT
ENST00000700200.1:n.191+2352_191+2354delinsCTT
ENST00000700201.1:c.68-198_68-196delinsCTT	ENSP00000514855.1:n.68-198_68-196delinsCTT
ENST00000380152.8:c.68-198_68-196delinsCTT MANE Select	ENSP00000369497.3:n.68-198_68-196delinsCTT
ENST00000544455.6:c.68-198_68-196delinsCTT	ENSP00000439902.1:n.68-198_68-196delinsCTT
ENST00000614259.2:c.68-198_68-196delinsCTT	ENSP00000506251.1:n.68-198_68-196delinsCTT
ENST00000680887.1:c.68-198_68-196delinsCTT	ENSP00000505508.1:n.68-198_68-196delinsCTT
ENST00000380152.7:c.68-198_68-196delinsCTT	ENSP00000369497.3:n.68-198_68-196delinsCTT
ENST00000530893.6:n.266-198_266-196delinsCTT
ENST00000544455.5:c.68-198_68-196delinsCTT	ENSP00000439902.1:n.68-198_68-196delinsCTT
ENST00000614259.1:n.68-198_68-196delinsCTT
NM_000059.3:c.68-198_68-196delinsCTT , LRG_293t1:c.68-198_68-196delinsCTT	NP_000050.2:n.68-198_68-196delinsCTT
XM_011535203.1:c.68-198_68-196delinsCTT	XP_011533505.1:n.68-198_68-196delinsCTT
XM_011535204.1:c.68-198_68-196delinsCTT	XP_011533506.1:n.68-198_68-196delinsCTT
XM_011535205.1:c.68-198_68-196delinsCTT	XP_011533507.1:n.68-198_68-196delinsCTT
NM_000059.4:c.68-198_68-196delinsCTT MANE Select	NP_000050.3:n.68-198_68-196delinsCTT