Canonical Allele Identifier: CA2082752887

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32326680_32326682delinsTTC , CM000675.2:g.32326680_32326682delinsTTC	GRCh38
NC_000013.10:g.32900817_32900819delinsTTC , CM000675.1:g.32900817_32900819delinsTTC	GRCh37
NC_000013.9:g.31798817_31798819delinsTTC	NCBI36
NG_012772.3:g.16201_16203delinsTTC , LRG_293:g.16201_16203delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.631+67_631+69delinsTTC	ENSP00000434898.2:n.631+67_631+69delinsTTC
ENST00000528762.2:c.631+67_631+69delinsTTC	ENSP00000433168.2:n.631+67_631+69delinsTTC
ENST00000530893.7:c.262+67_262+69delinsTTC	ENSP00000499438.2:n.262+67_262+69delinsTTC
ENST00000665585.2:c.631+67_631+69delinsTTC	ENSP00000499570.2:n.631+67_631+69delinsTTC
ENST00000666593.2:c.631+67_631+69delinsTTC	ENSP00000499256.2:n.631+67_631+69delinsTTC
ENST00000700202.2:c.631+67_631+69delinsTTC	ENSP00000514856.2:n.631+67_631+69delinsTTC
ENST00000700200.1:n.569_571delinsTTC
ENST00000700201.1:c.*410+67_*410+69delinsTTC	ENSP00000514855.1:n.*410+67_*410+69delinsTTC
ENST00000380152.8:c.631+67_631+69delinsTTC MANE Select	ENSP00000369497.3:n.631+67_631+69delinsTTC
ENST00000544455.6:c.631+67_631+69delinsTTC	ENSP00000439902.1:n.631+67_631+69delinsTTC
ENST00000614259.2:c.631+67_631+69delinsTTC	ENSP00000506251.1:n.631+67_631+69delinsTTC
ENST00000680887.1:c.631+67_631+69delinsTTC	ENSP00000505508.1:n.631+67_631+69delinsTTC
ENST00000380152.7:c.631+67_631+69delinsTTC	ENSP00000369497.3:n.631+67_631+69delinsTTC
ENST00000530893.6:n.829+67_829+69delinsTTC
ENST00000544455.5:c.631+67_631+69delinsTTC	ENSP00000439902.1:n.631+67_631+69delinsTTC
ENST00000614259.1:n.631+67_631+69delinsTTC
NM_000059.3:c.631+67_631+69delinsTTC , LRG_293t1:c.631+67_631+69delinsTTC	NP_000050.2:n.631+67_631+69delinsTTC
XM_011535203.1:c.631+67_631+69delinsTTC	XP_011533505.1:n.631+67_631+69delinsTTC
XM_011535204.1:c.631+67_631+69delinsTTC	XP_011533506.1:n.631+67_631+69delinsTTC
XM_011535205.1:c.631+67_631+69delinsTTC	XP_011533507.1:n.631+67_631+69delinsTTC
NM_000059.4:c.631+67_631+69delinsTTC MANE Select	NP_000050.3:n.631+67_631+69delinsTTC