Canonical Allele Identifier: CA2244533412
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916080075

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734142del , CM000679.2:g.4734142del GRCh38
NC_000017.10:g.4637437del , CM000679.1:g.4637437del GRCh37
NC_000017.9:g.4584186del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*365del MANE Select ENSP00000293778.7:n.*365del
ENST00000293778.10:c.*365del ENSP00000293778.6:n.*365del
ENST00000576153.5:n.921del
NM_022059.3:c.*365del NP_071342.2:n.*365del
NM_022059.4:c.*365del NP_071342.2:n.*365del
NM_001386809.1:c.*365del MANE Select NP_001373738.1:n.*365del