Canonical Allele Identifier: CA15432665
Gene: SLC22A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160353896A>G , CM000668.2:g.160353896A>G GRCh38
NC_000006.11:g.160774928A>G , CM000668.1:g.160774928A>G GRCh37
NC_000006.10:g.160694918A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000275300.3:c.429+5048A>G MANE Select ENSP00000275300.2:n.429+5048A>G
ENST00000275300.2:c.429+5048A>G ENSP00000275300.2:n.429+5048A>G
NM_021977.3:c.429+5048A>G NP_068812.1:n.429+5048A>G
XM_005267106.3:c.36+4838A>G XP_005267163.1:n.36+4838A>G
XM_005267107.2:c.429+5048A>G XP_005267164.1:n.429+5048A>G
XM_011536076.1:c.-28+4711A>G XP_011534378.1:n.-28+4711A>G
XM_011536077.1:c.-28+3226A>G XP_011534379.1:n.-28+3226A>G
XM_011536078.1:c.429+5048A>G XP_011534380.1:n.429+5048A>G
XR_245546.1:n.471+5048A>G
XM_005267106.5:c.36+4838A>G XP_005267163.1:n.36+4838A>G
XM_005267107.3:c.429+5048A>G XP_005267164.1:n.429+5048A>G
XM_011536076.3:c.-28+4711A>G XP_011534378.1:n.-28+4711A>G
XM_017011203.2:c.-28+3226A>G XP_016866692.1:n.-28+3226A>G
XR_001743588.1:n.471+5048A>G
XR_001743589.1:n.471+5048A>G
NM_021977.4:c.429+5048A>G MANE Select NP_068812.1:n.429+5048A>G
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