Canonical Allele Identifier: CA2635549583
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734037_4734038insA , CM000679.2:g.4734037_4734038insA GRCh38
NC_000017.10:g.4637332_4637333insA , CM000679.1:g.4637332_4637333insA GRCh37
NC_000017.9:g.4584081_4584082insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*465_*466insT MANE Select ENSP00000293778.7:n.*465_*466insT
ENST00000293778.10:c.*465_*466insT ENSP00000293778.6:n.*465_*466insT
ENST00000576153.5:n.1021_1022insT
NM_022059.3:c.*465_*466insT NP_071342.2:n.*465_*466insT
NM_022059.4:c.*465_*466insT NP_071342.2:n.*465_*466insT
NM_001386809.1:c.*465_*466insT MANE Select NP_001373738.1:n.*465_*466insT