Canonical Allele Identifier: CA2808290856
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734131_4734132insCAAAA , CM000679.2:g.4734131_4734132insCAAAA GRCh38
NC_000017.10:g.4637426_4637427insCAAAA , CM000679.1:g.4637426_4637427insCAAAA GRCh37
NC_000017.9:g.4584175_4584176insCAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*371_*372insTTTTG MANE Select ENSP00000293778.7:n.*371_*372insTTTTG
ENST00000293778.10:c.*371_*372insTTTTG ENSP00000293778.6:n.*371_*372insTTTTG
ENST00000576153.5:n.927_928insTTTTG
NM_022059.3:c.*371_*372insTTTTG NP_071342.2:n.*371_*372insTTTTG
NM_022059.4:c.*371_*372insTTTTG NP_071342.2:n.*371_*372insTTTTG
NM_001386809.1:c.*371_*372insTTTTG MANE Select NP_001373738.1:n.*371_*372insTTTTG