Canonical Allele Identifier: CA954689070

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32318452_32318453insTTTTTTTTTTTTTTTTTTTT , CM000675.2:g.32318452_32318453insTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000013.10:g.32892589_32892590insTTTTTTTTTTTTTTTTTTTT , CM000675.1:g.32892589_32892590insTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000013.9:g.31790589_31790590insTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_012772.3:g.7973_7974insTTTTTTTTTTTTTTTTTTTT , LRG_293:g.7973_7974insTTTTTTTTTTTTTTTTTTTT
NG_017006.2:g.1924_1925insAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000434898.2:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000528762.2:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000433168.2:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000530893.7:c.-302-625_-302-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000499438.2:n.-302-625_-302-624insTTTTTTTTTTTTTTTTTTTT
ENST00000665585.2:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000499570.2:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000666593.2:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000499256.2:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000700202.2:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000514856.2:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000700200.1:n.191+1925_191+1926insTTTTTTTTTTTTTTTTTTTT
ENST00000700201.1:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000514855.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000380152.8:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000369497.3:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000544455.6:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000439902.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000614259.2:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000506251.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000680887.1:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000505508.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000380152.7:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000369497.3:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000530893.6:n.266-625_266-624insTTTTTTTTTTTTTTTTTTTT
ENST00000544455.5:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	ENSP00000439902.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
ENST00000614259.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
NM_000059.3:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT , LRG_293t1:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	NP_000050.2:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
XM_011535203.1:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	XP_011533505.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
XM_011535204.1:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	XP_011533506.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
XM_011535205.1:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT	XP_011533507.1:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT
NM_000059.4:c.68-625_68-624insTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000050.3:n.68-625_68-624insTTTTTTTTTTTTTTTTTTTT