Canonical Allele Identifier: CA2727923887

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137661970

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398070_32398073del , CM000675.2:g.32398070_32398073del	GRCh38
NC_000013.10:g.32972207_32972210del , CM000675.1:g.32972207_32972210del	GRCh37
NC_000013.9:g.31870207_31870210del	NCBI36
NG_012772.3:g.87591_87594del , LRG_293:g.87591_87594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*172-92_*172-89del	ENSP00000434898.2:n.*172-92_*172-89del
ENST00000528762.2:c.*1016-92_*1016-89del	ENSP00000433168.2:n.*1016-92_*1016-89del
ENST00000530893.7:c.9280-92_9280-89del	ENSP00000499438.2:n.9280-92_9280-89del
ENST00000665585.2:c.*1211-92_*1211-89del	ENSP00000499570.2:n.*1211-92_*1211-89del
ENST00000700202.2:c.9598-92_9598-89del	ENSP00000514856.2:n.9598-92_9598-89del
ENST00000700202.1:c.2065-92_2065-89del	ENSP00000514856.1:n.2065-92_2065-89del
ENST00000700203.1:n.1776-92_1776-89del
ENST00000380152.8:c.9649-92_9649-89del MANE Select	ENSP00000369497.3:n.9649-92_9649-89del
ENST00000544455.6:c.9649-92_9649-89del	ENSP00000439902.1:n.9649-92_9649-89del
ENST00000614259.2:c.9657-92_9657-89del	ENSP00000506251.1:n.9657-92_9657-89del
ENST00000665585.1:c.2527-92_2527-89del
ENST00000680887.1:c.9649-92_9649-89del	ENSP00000505508.1:n.9649-92_9649-89del
ENST00000380152.7:c.9649-92_9649-89del	ENSP00000369497.3:n.9649-92_9649-89del
ENST00000470094.1:c.732-92_732-89del
ENST00000533776.1:n.237-92_237-89del
ENST00000544455.5:c.9649-92_9649-89del	ENSP00000439902.1:n.9649-92_9649-89del
NM_000059.3:c.9649-92_9649-89del , LRG_293t1:c.9649-92_9649-89del	NP_000050.2:n.9649-92_9649-89del
XM_011535203.1:c.9649-92_9649-89del	XP_011533505.1:n.9649-92_9649-89del
XM_011535204.1:c.9553-92_9553-89del	XP_011533506.1:n.9553-92_9553-89del
NM_000059.4:c.9649-92_9649-89del MANE Select	NP_000050.3:n.9649-92_9649-89del