Canonical Allele Identifier: CA2635549610
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734059del , CM000679.2:g.4734059del GRCh38
NC_000017.10:g.4637354del , CM000679.1:g.4637354del GRCh37
NC_000017.9:g.4584103del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*449del MANE Select ENSP00000293778.7:n.*449del
ENST00000293778.10:c.*449del ENSP00000293778.6:n.*449del
ENST00000576153.5:n.1005del
NM_022059.3:c.*449del NP_071342.2:n.*449del
NM_022059.4:c.*449del NP_071342.2:n.*449del
NM_001386809.1:c.*449del MANE Select NP_001373738.1:n.*449del