Canonical Allele Identifier: CA2082835630

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398380_32398381delinsTG , CM000675.2:g.32398380_32398381delinsTG	GRCh38
NC_000013.10:g.32972517_32972518delinsTG , CM000675.1:g.32972517_32972518delinsTG	GRCh37
NC_000013.9:g.31870517_31870518delinsTG	NCBI36
NG_012772.3:g.87901_87902delinsTG , LRG_293:g.87901_87902delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*390_*391delinsTG	ENSP00000434898.2:n.*390_*391delinsTG
ENST00000528762.2:c.*1234_*1235delinsTG	ENSP00000433168.2:n.*1234_*1235delinsTG
ENST00000530893.7:c.9498_9499delinsTG	ENSP00000499438.2:p.Phe3166=
ENST00000665585.2:c.*1429_*1430delinsTG	ENSP00000499570.2:n.*1429_*1430delinsTG
ENST00000700202.2:c.9816_9817delinsTG	ENSP00000514856.2:p.Phe3272=
ENST00000700202.1:c.2283_2284delinsTG	ENSP00000514856.1:p.Phe761=
ENST00000700203.1:n.1994_1995delinsTG
ENST00000380152.8:c.9867_9868delinsTG MANE Select	ENSP00000369497.3:p.Phe3289=
ENST00000544455.6:c.9867_9868delinsTG	ENSP00000439902.1:p.Phe3289=
ENST00000614259.2:c.9875_9876delinsTG	ENSP00000506251.1:n.9875_9876delinsTG
ENST00000680887.1:c.9867_9868delinsTG	ENSP00000505508.1:p.Phe3289=
ENST00000380152.7:c.9867_9868delinsTG	ENSP00000369497.3:p.Phe3289=
ENST00000533776.1:n.455_456delinsTG
ENST00000544455.5:c.9867_9868delinsTG	ENSP00000439902.1:p.Phe3289=
NM_000059.3:c.9867_9868delinsTG , LRG_293t1:c.9867_9868delinsTG	NP_000050.2:p.Phe3289=
XM_011535203.1:c.9867_9868delinsTG	XP_011533505.1:p.Phe3289=
XM_011535204.1:c.9771_9772delinsTG	XP_011533506.1:p.Phe3257=
NM_000059.4:c.9867_9868delinsTG MANE Select	NP_000050.3:p.Phe3289=