Canonical Allele Identifier: CA2576133298
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734532del , CM000679.2:g.4734532del GRCh38
NC_000017.10:g.4637827del , CM000679.1:g.4637827del GRCh37
NC_000017.9:g.4584576del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*23+51del MANE Select ENSP00000293778.7:n.*23+51del
ENST00000574412.6:c.*74del ENSP00000459592.2:n.*74del
ENST00000293778.10:c.*23+51del ENSP00000293778.6:n.*23+51del
ENST00000574412.5:c.*74del ENSP00000459592.1:n.*74del
ENST00000576153.5:n.579+51del
NM_001100812.1:c.*74del NP_001094282.1:n.*74del
NM_022059.3:c.*23+51del NP_071342.2:n.*23+51del
NM_022059.4:c.*23+51del NP_071342.2:n.*23+51del
NM_001100812.2:c.*74del NP_001094282.2:n.*74del
NM_001386809.1:c.*23+51del MANE Select NP_001373738.1:n.*23+51del