Canonical Allele Identifier: CA2244533486
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734192_4734194delinsCGA , CM000679.2:g.4734192_4734194delinsCGA GRCh38
NC_000017.10:g.4637487_4637489delinsCGA , CM000679.1:g.4637487_4637489delinsCGA GRCh37
NC_000017.9:g.4584236_4584238delinsCGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*309_*311delinsTCG MANE Select ENSP00000293778.7:n.*309_*311delinsTCG
ENST00000293778.10:c.*309_*311delinsTCG ENSP00000293778.6:n.*309_*311delinsTCG
ENST00000576153.5:n.865_867delinsTCG
NM_022059.3:c.*309_*311delinsTCG NP_071342.2:n.*309_*311delinsTCG
NM_022059.4:c.*309_*311delinsTCG NP_071342.2:n.*309_*311delinsTCG
NM_001386809.1:c.*309_*311delinsTCG MANE Select NP_001373738.1:n.*309_*311delinsTCG