Canonical Allele Identifier: CA2244533902
Gene: CXCL16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734468T= , CM000679.2:g.4734468T= GRCh38
NC_000017.10:g.4637763T= , CM000679.1:g.4637763T= GRCh37
NC_000017.9:g.4584512T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*35A= MANE Select ENSP00000293778.7:n.*35A=
ENST00000574412.6:c.*138A= ENSP00000459592.2:n.*138A=
ENST00000293778.10:c.*35A= ENSP00000293778.6:n.*35A=
ENST00000574412.5:c.*138A= ENSP00000459592.1:n.*138A=
ENST00000576153.5:n.591A=
NM_022059.3:c.*35A= NP_071342.2:n.*35A=
NM_022059.4:c.*35A= NP_071342.2:n.*35A=
NM_001386809.1:c.*35A= MANE Select NP_001373738.1:n.*35A=
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