Canonical Allele Identifier: CA2244533778
Gene: CXCL16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734401T= , CM000679.2:g.4734401T= GRCh38
NC_000017.10:g.4637696T= , CM000679.1:g.4637696T= GRCh37
NC_000017.9:g.4584445T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*102A= MANE Select ENSP00000293778.7:n.*102A=
ENST00000574412.6:c.*205A= ENSP00000459592.2:n.*205A=
ENST00000293778.10:c.*102A= ENSP00000293778.6:n.*102A=
ENST00000574412.5:c.*205A= ENSP00000459592.1:n.*205A=
ENST00000576153.5:n.658A=
NM_022059.3:c.*102A= NP_071342.2:n.*102A=
NM_022059.4:c.*102A= NP_071342.2:n.*102A=
NM_001386809.1:c.*102A= MANE Select NP_001373738.1:n.*102A=
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