Canonical Allele Identifier: CA143346317

Gene: BACH2

Linked Data

• dbSNP Id: rs376976228

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.89988728_89988731del , CM000668.2:g.89988728_89988731del	GRCh38
NC_000006.11:g.90698447_90698450del , CM000668.1:g.90698447_90698450del	GRCh37
NC_000006.10:g.90755168_90755171del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406998.7:c.243+19874_243+19877del	ENSP00000384145.3:n.243+19874_243+19877del
ENST00000453877.6:c.243+19874_243+19877del	ENSP00000397668.2:n.243+19874_243+19877del
ENST00000695952.1:c.243+19874_243+19877del	ENSP00000512284.1:n.243+19874_243+19877del
ENST00000695953.1:n.1093+19874_1093+19877del
ENST00000695954.1:n.336-12825_336-12822del
ENST00000257749.9:c.243+19874_243+19877del MANE Select	ENSP00000257749.4:n.243+19874_243+19877del
ENST00000257749.8:c.243+19874_243+19877del	ENSP00000257749.4:n.243+19874_243+19877del
ENST00000343122.7:c.243+19874_243+19877del	ENSP00000345642.3:n.243+19874_243+19877del
ENST00000537989.5:c.243+19874_243+19877del	ENSP00000437473.1:n.243+19874_243+19877del
NM_001170794.1:c.243+19874_243+19877del	NP_001164265.1:n.243+19874_243+19877del
NM_021813.3:c.243+19874_243+19877del	NP_068585.1:n.243+19874_243+19877del
XM_005248758.3:c.351+19874_351+19877del	XP_005248815.1:n.351+19874_351+19877del
XM_005248759.3:c.243+19874_243+19877del	XP_005248816.1:n.243+19874_243+19877del
XM_011536037.1:c.243+19874_243+19877del	XP_011534339.1:n.243+19874_243+19877del
XM_011536038.1:c.243+19874_243+19877del	XP_011534340.1:n.243+19874_243+19877del
XM_011536039.1:c.243+19874_243+19877del	XP_011534341.1:n.243+19874_243+19877del
XM_011536040.1:c.243+19874_243+19877del	XP_011534342.1:n.243+19874_243+19877del
XM_011536041.1:c.243+19874_243+19877del	XP_011534343.1:n.243+19874_243+19877del
XM_011536042.1:c.549+19874_549+19877del	XP_011534344.1:n.549+19874_549+19877del
XM_011536043.1:c.549+19874_549+19877del	XP_011534345.1:n.549+19874_549+19877del
XM_005248758.5:c.351+19874_351+19877del	XP_005248815.1:n.351+19874_351+19877del
XM_005248759.5:c.243+19874_243+19877del	XP_005248816.1:n.243+19874_243+19877del
XM_011536039.3:c.243+19874_243+19877del	XP_011534341.1:n.243+19874_243+19877del
XM_011536040.2:c.243+19874_243+19877del	XP_011534342.1:n.243+19874_243+19877del
XM_017011166.2:c.243+19874_243+19877del	XP_016866655.1:n.243+19874_243+19877del
XM_017011167.2:c.501+19874_501+19877del	XP_016866656.1:n.501+19874_501+19877del
XM_024446510.1:c.501+19874_501+19877del	XP_024302278.1:n.501+19874_501+19877del
XM_024446511.1:c.501+19874_501+19877del	XP_024302279.1:n.501+19874_501+19877del
XM_024446513.1:c.243+19874_243+19877del	XP_024302281.1:n.243+19874_243+19877del
NM_021813.4:c.243+19874_243+19877del MANE Select	NP_068585.1:n.243+19874_243+19877del
NM_001170794.2:c.243+19874_243+19877del	NP_001164265.1:n.243+19874_243+19877del