Canonical Allele Identifier: CA2082817020

Gene: BRCA2

Linked Data

• dbSNP Id: rs2072706166

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357549_32357550insCTGTACATTTATATTT , CM000675.2:g.32357549_32357550insCTGTACATTTATATTT	GRCh38
NC_000013.10:g.32931686_32931687insCTGTACATTTATATTT , CM000675.1:g.32931686_32931687insCTGTACATTTATATTT	GRCh37
NC_000013.9:g.31829686_31829687insCTGTACATTTATATTT	NCBI36
NG_012772.3:g.47070_47071insCTGTACATTTATATTT , LRG_293:g.47070_47071insCTGTACATTTATATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000434898.2:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000528762.2:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000433168.2:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000530893.7:c.7249-193_7249-192insCTGTACATTTATATTT	ENSP00000499438.2:n.7249-193_7249-192insCTGTACATTTATATTT
ENST00000665585.2:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000499570.2:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000666593.2:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000499256.2:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000700202.2:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000514856.2:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000700202.1:c.85-193_85-192insCTGTACATTTATATTT	ENSP00000514856.1:n.85-193_85-192insCTGTACATTTATATTT
ENST00000380152.8:c.7618-193_7618-192insCTGTACATTTATATTT MANE Select	ENSP00000369497.3:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000544455.6:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000439902.1:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000614259.2:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000506251.1:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000665585.1:c.183-193_183-192insCTGTACATTTATATTT
ENST00000680887.1:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000505508.1:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000380152.7:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000369497.3:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000544455.5:c.7618-193_7618-192insCTGTACATTTATATTT	ENSP00000439902.1:n.7618-193_7618-192insCTGTACATTTATATTT
ENST00000614259.1:n.7618-193_7618-192insCTGTACATTTATATTT
NM_000059.3:c.7618-193_7618-192insCTGTACATTTATATTT , LRG_293t1:c.7618-193_7618-192insCTGTACATTTATATTT	NP_000050.2:n.7618-193_7618-192insCTGTACATTTATATTT
XM_011535203.1:c.7618-193_7618-192insCTGTACATTTATATTT	XP_011533505.1:n.7618-193_7618-192insCTGTACATTTATATTT
XM_011535204.1:c.7522-193_7522-192insCTGTACATTTATATTT	XP_011533506.1:n.7522-193_7522-192insCTGTACATTTATATTT
XM_011535205.1:c.7618-193_7618-192insCTGTACATTTATATTT	XP_011533507.1:n.7618-193_7618-192insCTGTACATTTATATTT
NM_000059.4:c.7618-193_7618-192insCTGTACATTTATATTT MANE Select	NP_000050.3:n.7618-193_7618-192insCTGTACATTTATATTT