Canonical Allele Identifier: CA1645671793
Gene: BACH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.89931162_89931163delinsAG , CM000668.2:g.89931162_89931163delinsAG GRCh38
NC_000006.11:g.90640881_90640882delinsAG , CM000668.1:g.90640881_90640882delinsAG GRCh37
NC_000006.10:g.90697602_90697603delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257749.9:c.*1245_*1246delinsCT MANE Select ENSP00000257749.4:n.*1245_*1246delinsCT
ENST00000257749.8:c.*1245_*1246delinsCT ENSP00000257749.4:n.*1245_*1246delinsCT
ENST00000537989.5:c.*1245_*1246delinsCT ENSP00000437473.1:n.*1245_*1246delinsCT
NM_001170794.1:c.*1245_*1246delinsCT NP_001164265.1:n.*1245_*1246delinsCT
NM_021813.3:c.*1245_*1246delinsCT NP_068585.1:n.*1245_*1246delinsCT
XM_005248758.3:c.*1245_*1246delinsCT XP_005248815.1:n.*1245_*1246delinsCT
XM_005248759.3:c.*1245_*1246delinsCT XP_005248816.1:n.*1245_*1246delinsCT
XM_011536037.1:c.*1245_*1246delinsCT XP_011534339.1:n.*1245_*1246delinsCT
XM_011536038.1:c.*1245_*1246delinsCT XP_011534340.1:n.*1245_*1246delinsCT
XM_011536039.1:c.*1245_*1246delinsCT XP_011534341.1:n.*1245_*1246delinsCT
XM_011536040.1:c.*1245_*1246delinsCT XP_011534342.1:n.*1245_*1246delinsCT
XM_011536041.1:c.*1245_*1246delinsCT XP_011534343.1:n.*1245_*1246delinsCT
XM_005248758.5:c.*1245_*1246delinsCT XP_005248815.1:n.*1245_*1246delinsCT
XM_005248759.5:c.*1245_*1246delinsCT XP_005248816.1:n.*1245_*1246delinsCT
XM_017011166.2:c.*1245_*1246delinsCT XP_016866655.1:n.*1245_*1246delinsCT
XM_024446510.1:c.*1245_*1246delinsCT XP_024302278.1:n.*1245_*1246delinsCT
XM_024446511.1:c.*1245_*1246delinsCT XP_024302279.1:n.*1245_*1246delinsCT
NM_021813.4:c.*1245_*1246delinsCT MANE Select NP_068585.1:n.*1245_*1246delinsCT
NM_001170794.2:c.*1245_*1246delinsCT NP_001164265.1:n.*1245_*1246delinsCT