Canonical Allele Identifier: CA2635549599
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734050dup , CM000679.2:g.4734050dup GRCh38
NC_000017.10:g.4637345dup , CM000679.1:g.4637345dup GRCh37
NC_000017.9:g.4584094dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*457dup MANE Select ENSP00000293778.7:n.*457dup
ENST00000293778.10:c.*457dup ENSP00000293778.6:n.*457dup
ENST00000576153.5:n.1013dup
NM_022059.3:c.*457dup NP_071342.2:n.*457dup
NM_022059.4:c.*457dup NP_071342.2:n.*457dup
NM_001386809.1:c.*457dup MANE Select NP_001373738.1:n.*457dup