Canonical Allele Identifier: CA2244533872
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734447_4734448delinsTC , CM000679.2:g.4734447_4734448delinsTC GRCh38
NC_000017.10:g.4637742_4637743delinsTC , CM000679.1:g.4637742_4637743delinsTC GRCh37
NC_000017.9:g.4584491_4584492delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*55_*56delinsGA MANE Select ENSP00000293778.7:n.*55_*56delinsGA
ENST00000574412.6:c.*158_*159delinsGA ENSP00000459592.2:n.*158_*159delinsGA
ENST00000293778.10:c.*55_*56delinsGA ENSP00000293778.6:n.*55_*56delinsGA
ENST00000574412.5:c.*158_*159delinsGA ENSP00000459592.1:n.*158_*159delinsGA
ENST00000576153.5:n.611_612delinsGA
NM_022059.3:c.*55_*56delinsGA NP_071342.2:n.*55_*56delinsGA
NM_022059.4:c.*55_*56delinsGA NP_071342.2:n.*55_*56delinsGA
NM_001386809.1:c.*55_*56delinsGA MANE Select NP_001373738.1:n.*55_*56delinsGA