Canonical Allele Identifier: CA2082809415
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32338564_32338569delinsTTCAAA , CM000675.2:g.32338564_32338569delinsTTCAAA GRCh38
NC_000013.10:g.32912701_32912706delinsTTCAAA , CM000675.1:g.32912701_32912706delinsTTCAAA GRCh37
NC_000013.9:g.31810701_31810706delinsTTCAAA NCBI36
NG_012772.3:g.28085_28090delinsTTCAAA , LRG_293:g.28085_28090delinsTTCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.4209_4214delinsTTCAAA ENSP00000434898.2:p.Thr1403=
ENST00000528762.2:c.4209_4214delinsTTCAAA ENSP00000433168.2:p.Thr1403=
ENST00000530893.7:c.3840_3845delinsTTCAAA ENSP00000499438.2:p.Thr1280=
ENST00000665585.2:c.4209_4214delinsTTCAAA ENSP00000499570.2:p.Thr1403=
ENST00000666593.2:c.4209_4214delinsTTCAAA ENSP00000499256.2:p.Thr1403=
ENST00000700202.2:c.4209_4214delinsTTCAAA ENSP00000514856.2:p.Thr1403=
ENST00000380152.8:c.4209_4214delinsTTCAAA MANE Select ENSP00000369497.3:p.Thr1403=
ENST00000544455.6:c.4209_4214delinsTTCAAA ENSP00000439902.1:p.Thr1403=
ENST00000614259.2:c.4209_4214delinsTTCAAA ENSP00000506251.1:p.Thr1403=
ENST00000680887.1:c.4209_4214delinsTTCAAA ENSP00000505508.1:p.Thr1403=
ENST00000380152.7:c.4209_4214delinsTTCAAA ENSP00000369497.3:p.Thr1403=
ENST00000544455.5:c.4209_4214delinsTTCAAA ENSP00000439902.1:p.Thr1403=
ENST00000614259.1:n.4209_4214delinsTTCAAA
NM_000059.3:c.4209_4214delinsTTCAAA , LRG_293t1:c.4209_4214delinsTTCAAA NP_000050.2:p.Thr1403=
XM_011535203.1:c.4209_4214delinsTTCAAA XP_011533505.1:p.Thr1403=
XM_011535204.1:c.4209_4214delinsTTCAAA XP_011533506.1:p.Thr1403=
XM_011535205.1:c.4209_4214delinsTTCAAA XP_011533507.1:p.Thr1403=
NM_000059.4:c.4209_4214delinsTTCAAA MANE Select NP_000050.3:p.Thr1403=