Canonical Allele Identifier: CA2635549629
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734068del , CM000679.2:g.4734068del GRCh38
NC_000017.10:g.4637363del , CM000679.1:g.4637363del GRCh37
NC_000017.9:g.4584112del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*437del MANE Select ENSP00000293778.7:n.*437del
ENST00000293778.10:c.*437del ENSP00000293778.6:n.*437del
ENST00000576153.5:n.993del
NM_022059.3:c.*437del NP_071342.2:n.*437del
NM_022059.4:c.*437del NP_071342.2:n.*437del
NM_001386809.1:c.*437del MANE Select NP_001373738.1:n.*437del