Canonical Allele Identifier: CA2082809916
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32355079_32355080delinsCT , CM000675.2:g.32355079_32355080delinsCT GRCh38
NC_000013.10:g.32929216_32929217delinsCT , CM000675.1:g.32929216_32929217delinsCT GRCh37
NC_000013.9:g.31827216_31827217delinsCT NCBI36
NG_012772.3:g.44600_44601delinsCT , LRG_293:g.44600_44601delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7226_7227delinsCT ENSP00000434898.2:p.Pro2409=
ENST00000528762.2:c.7226_7227delinsCT ENSP00000433168.2:p.Pro2409=
ENST00000530893.7:c.6857_6858delinsCT ENSP00000499438.2:p.Pro2286=
ENST00000665585.2:c.7226_7227delinsCT ENSP00000499570.2:p.Pro2409=
ENST00000666593.2:c.7226_7227delinsCT ENSP00000499256.2:p.Pro2409=
ENST00000700202.2:c.7226_7227delinsCT ENSP00000514856.2:p.Pro2409=
ENST00000380152.8:c.7226_7227delinsCT MANE Select ENSP00000369497.3:p.Pro2409=
ENST00000544455.6:c.7226_7227delinsCT ENSP00000439902.1:p.Pro2409=
ENST00000614259.2:c.7226_7227delinsCT ENSP00000506251.1:p.Pro2409=
ENST00000680887.1:c.7226_7227delinsCT ENSP00000505508.1:p.Pro2409=
ENST00000380152.7:c.7226_7227delinsCT ENSP00000369497.3:p.Pro2409=
ENST00000544455.5:c.7226_7227delinsCT ENSP00000439902.1:p.Pro2409=
ENST00000614259.1:n.7226_7227delinsCT
NM_000059.3:c.7226_7227delinsCT , LRG_293t1:c.7226_7227delinsCT NP_000050.2:p.Pro2409=
XM_011535203.1:c.7226_7227delinsCT XP_011533505.1:p.Pro2409=
XM_011535204.1:c.7130_7131delinsCT XP_011533506.1:p.Pro2377=
XM_011535205.1:c.7226_7227delinsCT XP_011533507.1:p.Pro2409=
NM_000059.4:c.7226_7227delinsCT MANE Select NP_000050.3:p.Pro2409=