Canonical Allele Identifier: CA2082814124
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340760_32340767delinsCTTAAATG , CM000675.2:g.32340760_32340767delinsCTTAAATG GRCh38
NC_000013.10:g.32914897_32914904delinsCTTAAATG , CM000675.1:g.32914897_32914904delinsCTTAAATG GRCh37
NC_000013.9:g.31812897_31812904delinsCTTAAATG NCBI36
NG_012772.3:g.30281_30288delinsCTTAAATG , LRG_293:g.30281_30288delinsCTTAAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.6405_6412delinsCTTAAATG ENSP00000434898.2:p.Asn2135=
ENST00000528762.2:c.6405_6412delinsCTTAAATG ENSP00000433168.2:p.Asn2135=
ENST00000530893.7:c.6036_6043delinsCTTAAATG ENSP00000499438.2:p.Asn2012=
ENST00000665585.2:c.6405_6412delinsCTTAAATG ENSP00000499570.2:p.Asn2135=
ENST00000666593.2:c.6405_6412delinsCTTAAATG ENSP00000499256.2:p.Asn2135=
ENST00000700202.2:c.6405_6412delinsCTTAAATG ENSP00000514856.2:p.Asn2135=
ENST00000380152.8:c.6405_6412delinsCTTAAATG MANE Select ENSP00000369497.3:p.Asn2135=
ENST00000544455.6:c.6405_6412delinsCTTAAATG ENSP00000439902.1:p.Asn2135=
ENST00000614259.2:c.6405_6412delinsCTTAAATG ENSP00000506251.1:p.Asn2135=
ENST00000680887.1:c.6405_6412delinsCTTAAATG ENSP00000505508.1:p.Asn2135=
ENST00000380152.7:c.6405_6412delinsCTTAAATG ENSP00000369497.3:p.Asn2135=
ENST00000544455.5:c.6405_6412delinsCTTAAATG ENSP00000439902.1:p.Asn2135=
ENST00000614259.1:n.6405_6412delinsCTTAAATG
NM_000059.3:c.6405_6412delinsCTTAAATG , LRG_293t1:c.6405_6412delinsCTTAAATG NP_000050.2:p.Asn2135=
XM_011535203.1:c.6405_6412delinsCTTAAATG XP_011533505.1:p.Asn2135=
XM_011535204.1:c.6405_6412delinsCTTAAATG XP_011533506.1:p.Asn2135=
XM_011535205.1:c.6405_6412delinsCTTAAATG XP_011533507.1:p.Asn2135=
NM_000059.4:c.6405_6412delinsCTTAAATG MANE Select NP_000050.3:p.Asn2135=