Canonical Allele Identifier: CA1139770792
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32338443dup , CM000675.2:g.32338443dup GRCh38
NC_000013.10:g.32912580dup , CM000675.1:g.32912580dup GRCh37
NC_000013.9:g.31810580dup NCBI36
NG_012772.3:g.27964dup , LRG_293:g.27964dup

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.4088dup ENSP00000434898.2:p.Asn1363LysfsTer5
ENST00000528762.2:c.4088dup ENSP00000433168.2:p.Asn1363LysfsTer5
ENST00000530893.7:c.3719dup ENSP00000499438.2:p.Asn1240LysfsTer5
ENST00000665585.2:c.4088dup ENSP00000499570.2:p.Asn1363LysfsTer5
ENST00000666593.2:c.4088dup ENSP00000499256.2:p.Asn1363LysfsTer5
ENST00000700202.2:c.4088dup ENSP00000514856.2:p.Asn1363LysfsTer5
ENST00000380152.8:c.4088dup MANE Select ENSP00000369497.3:p.Asn1363LysfsTer5
ENST00000544455.6:c.4088dup ENSP00000439902.1:p.Asn1363LysfsTer5
ENST00000614259.2:c.4088dup ENSP00000506251.1:p.Asn1363LysfsTer5
ENST00000680887.1:c.4088dup ENSP00000505508.1:p.Asn1363LysfsTer5
ENST00000380152.7:c.4088dup ENSP00000369497.3:p.Asn1363LysfsTer5
ENST00000544455.5:c.4088dup ENSP00000439902.1:p.Asn1363LysfsTer5
ENST00000614259.1:n.4088dup
NM_000059.3:c.4088dup , LRG_293t1:c.4088dup NP_000050.2:p.Asn1363LysfsTer5
XM_011535203.1:c.4088dup XP_011533505.1:p.Asn1363LysfsTer5
XM_011535204.1:c.4088dup XP_011533506.1:p.Asn1363LysfsTer5
XM_011535205.1:c.4088dup XP_011533507.1:p.Asn1363LysfsTer5
NM_000059.4:c.4088dup MANE Select NP_000050.3:p.Asn1363LysfsTer5