Canonical Allele Identifier: CA1645781044

Gene: BACH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90170600_90170601delinsTA , CM000668.2:g.90170600_90170601delinsTA	GRCh38
NC_000006.11:g.90880319_90880320delinsTA , CM000668.1:g.90880319_90880320delinsTA	GRCh37
NC_000006.10:g.90937040_90937041delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406998.7:c.-162+35968_-162+35969delinsTA	ENSP00000384145.3:n.-162+35968_-162+35969delinsTA
ENST00000453877.6:c.-162+35968_-162+35969delinsTA	ENSP00000397668.2:n.-162+35968_-162+35969delinsTA
ENST00000470301.6:n.469+35968_469+35969delinsTA
ENST00000695952.1:c.-242+35968_-242+35969delinsTA	ENSP00000512284.1:n.-242+35968_-242+35969delinsTA
ENST00000695953.1:n.474+35968_474+35969delinsTA
ENST00000257749.9:c.-162+35968_-162+35969delinsTA MANE Select	ENSP00000257749.4:n.-162+35968_-162+35969delinsTA
ENST00000257749.8:c.-162+35968_-162+35969delinsTA	ENSP00000257749.4:n.-162+35968_-162+35969delinsTA
ENST00000343122.7:c.-162+35968_-162+35969delinsTA	ENSP00000345642.3:n.-162+35968_-162+35969delinsTA
ENST00000406998.6:c.-162+35968_-162+35969delinsTA	ENSP00000384145.2:n.-162+35968_-162+35969delinsTA
ENST00000453877.5:c.-162+35968_-162+35969delinsTA	ENSP00000397668.1:n.-162+35968_-162+35969delinsTA
ENST00000470301.5:n.469+35968_469+35969delinsTA
ENST00000472023.5:n.454+35968_454+35969delinsTA
ENST00000493201.5:n.380+35968_380+35969delinsTA
ENST00000494747.2:n.469+35968_469+35969delinsTA
ENST00000537989.5:c.-162+35968_-162+35969delinsTA	ENSP00000437473.1:n.-162+35968_-162+35969delinsTA
NM_001170794.1:c.-162+35968_-162+35969delinsTA	NP_001164265.1:n.-162+35968_-162+35969delinsTA
NM_021813.3:c.-162+35968_-162+35969delinsTA	NP_068585.1:n.-162+35968_-162+35969delinsTA
XM_011536037.1:c.-162+35968_-162+35969delinsTA	XP_011534339.1:n.-162+35968_-162+35969delinsTA
XM_011536038.1:c.-242+35968_-242+35969delinsTA	XP_011534340.1:n.-242+35968_-242+35969delinsTA
XM_011536039.1:c.-162+35968_-162+35969delinsTA	XP_011534341.1:n.-162+35968_-162+35969delinsTA
XM_011536040.1:c.-162+35968_-162+35969delinsTA	XP_011534342.1:n.-162+35968_-162+35969delinsTA
XM_011536041.1:c.-162+35968_-162+35969delinsTA	XP_011534343.1:n.-162+35968_-162+35969delinsTA
XM_011536042.1:c.65+2985_65+2986delinsTA	XP_011534344.1:n.65+2985_65+2986delinsTA
XM_011536043.1:c.65+2985_65+2986delinsTA	XP_011534345.1:n.65+2985_65+2986delinsTA
XM_011536039.3:c.-162+35968_-162+35969delinsTA	XP_011534341.1:n.-162+35968_-162+35969delinsTA
XM_011536040.2:c.-162+35968_-162+35969delinsTA	XP_011534342.1:n.-162+35968_-162+35969delinsTA
XM_017011166.2:c.-242+35968_-242+35969delinsTA	XP_016866655.1:n.-242+35968_-242+35969delinsTA
XM_017011167.2:c.-872+35968_-872+35969delinsTA	XP_016866656.1:n.-872+35968_-872+35969delinsTA
XM_024446513.1:c.-162+35968_-162+35969delinsTA	XP_024302281.1:n.-162+35968_-162+35969delinsTA
NM_021813.4:c.-162+35968_-162+35969delinsTA MANE Select	NP_068585.1:n.-162+35968_-162+35969delinsTA
NM_001170794.2:c.-162+35968_-162+35969delinsTA	NP_001164265.1:n.-162+35968_-162+35969delinsTA