Canonical Allele Identifier: CA2082834614
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32363230_32363232delinsGGA , CM000675.2:g.32363230_32363232delinsGGA GRCh38
NC_000013.10:g.32937367_32937369delinsGGA , CM000675.1:g.32937367_32937369delinsGGA GRCh37
NC_000013.9:g.31835367_31835369delinsGGA NCBI36
NG_012772.3:g.52751_52753delinsGGA , LRG_293:g.52751_52753delinsGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8028_8030delinsGGA ENSP00000434898.2:p.Met2676=
ENST00000528762.2:c.8028_8030delinsGGA ENSP00000433168.2:p.Met2676=
ENST00000530893.7:c.7659_7661delinsGGA ENSP00000499438.2:p.Met2553=
ENST00000665585.2:c.8028_8030delinsGGA ENSP00000499570.2:p.Met2676=
ENST00000666593.2:c.8028_8030delinsGGA ENSP00000499256.2:p.Met2676=
ENST00000700202.2:c.8028_8030delinsGGA ENSP00000514856.2:p.Met2676=
ENST00000700202.1:c.495_497delinsGGA ENSP00000514856.1:p.Met165=
ENST00000380152.8:c.8028_8030delinsGGA MANE Select ENSP00000369497.3:p.Met2676=
ENST00000544455.6:c.8028_8030delinsGGA ENSP00000439902.1:p.Met2676=
ENST00000614259.2:c.8036_8038delinsGGA ENSP00000506251.1:n.8036_8038delinsGGA
ENST00000665585.1:c.593_595delinsGGA
ENST00000680887.1:c.8028_8030delinsGGA ENSP00000505508.1:p.Met2676=
ENST00000380152.7:c.8028_8030delinsGGA ENSP00000369497.3:p.Met2676=
ENST00000544455.5:c.8028_8030delinsGGA ENSP00000439902.1:p.Met2676=
NM_000059.3:c.8028_8030delinsGGA , LRG_293t1:c.8028_8030delinsGGA NP_000050.2:p.Met2676=
XM_011535203.1:c.8028_8030delinsGGA XP_011533505.1:p.Met2676=
XM_011535204.1:c.7932_7934delinsGGA XP_011533506.1:p.Met2644=
XM_011535205.1:c.8028_8030delinsGGA XP_011533507.1:p.Met2676=
NM_000059.4:c.8028_8030delinsGGA MANE Select NP_000050.3:p.Met2676=