Canonical Allele Identifier: CA2772107592
Gene: BACH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.89930845_89930867dup , CM000668.2:g.89930845_89930867dup GRCh38
NC_000006.11:g.90640564_90640586dup , CM000668.1:g.90640564_90640586dup GRCh37
NC_000006.10:g.90697285_90697307dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257749.9:c.*1546_*1568dup MANE Select ENSP00000257749.4:n.*1546_*1568dup
ENST00000257749.8:c.*1546_*1568dup ENSP00000257749.4:n.*1546_*1568dup
ENST00000537989.5:c.*1546_*1568dup ENSP00000437473.1:n.*1546_*1568dup
NM_001170794.1:c.*1546_*1568dup NP_001164265.1:n.*1546_*1568dup
NM_021813.3:c.*1546_*1568dup NP_068585.1:n.*1546_*1568dup
XM_005248758.3:c.*1546_*1568dup XP_005248815.1:n.*1546_*1568dup
XM_005248759.3:c.*1546_*1568dup XP_005248816.1:n.*1546_*1568dup
XM_011536037.1:c.*1546_*1568dup XP_011534339.1:n.*1546_*1568dup
XM_011536038.1:c.*1546_*1568dup XP_011534340.1:n.*1546_*1568dup
XM_011536039.1:c.*1546_*1568dup XP_011534341.1:n.*1546_*1568dup
XM_011536040.1:c.*1546_*1568dup XP_011534342.1:n.*1546_*1568dup
XM_011536041.1:c.*1546_*1568dup XP_011534343.1:n.*1546_*1568dup
XM_005248758.5:c.*1546_*1568dup XP_005248815.1:n.*1546_*1568dup
XM_005248759.5:c.*1546_*1568dup XP_005248816.1:n.*1546_*1568dup
XM_017011166.2:c.*1546_*1568dup XP_016866655.1:n.*1546_*1568dup
XM_024446510.1:c.*1546_*1568dup XP_024302278.1:n.*1546_*1568dup
XM_024446511.1:c.*1546_*1568dup XP_024302279.1:n.*1546_*1568dup
NM_021813.4:c.*1546_*1568dup MANE Select NP_068585.1:n.*1546_*1568dup
NM_001170794.2:c.*1546_*1568dup NP_001164265.1:n.*1546_*1568dup