Canonical Allele Identifier: CA2635550255
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734528_4734530del , CM000679.2:g.4734528_4734530del GRCh38
NC_000017.10:g.4637823_4637825del , CM000679.1:g.4637823_4637825del GRCh37
NC_000017.9:g.4584572_4584574del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-48_*24-46del MANE Select ENSP00000293778.7:n.*24-48_*24-46del
ENST00000574412.6:c.*79_*81del ENSP00000459592.2:n.*79_*81del
ENST00000293778.10:c.*24-48_*24-46del ENSP00000293778.6:n.*24-48_*24-46del
ENST00000574412.5:c.*79_*81del ENSP00000459592.1:n.*79_*81del
ENST00000576153.5:n.580-48_580-46del
NM_001100812.1:c.*79_*81del NP_001094282.1:n.*79_*81del
NM_022059.3:c.*24-48_*24-46del NP_071342.2:n.*24-48_*24-46del
NM_022059.4:c.*24-48_*24-46del NP_071342.2:n.*24-48_*24-46del
NM_001100812.2:c.*79_*81del NP_001094282.2:n.*79_*81del
NM_001386809.1:c.*24-48_*24-46del MANE Select NP_001373738.1:n.*24-48_*24-46del