Canonical Allele Identifier: CA2635549959
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734225_4734228del , CM000679.2:g.4734225_4734228del GRCh38
NC_000017.10:g.4637520_4637523del , CM000679.1:g.4637520_4637523del GRCh37
NC_000017.9:g.4584269_4584272del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*278_*281del MANE Select ENSP00000293778.7:n.*278_*281del
ENST00000293778.10:c.*278_*281del ENSP00000293778.6:n.*278_*281del
ENST00000576153.5:n.834_837del
NM_022059.3:c.*278_*281del NP_071342.2:n.*278_*281del
NM_022059.4:c.*278_*281del NP_071342.2:n.*278_*281del
NM_001386809.1:c.*278_*281del MANE Select NP_001373738.1:n.*278_*281del