Canonical Allele Identifier: CA2808290888
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734536del , CM000679.2:g.4734536del GRCh38
NC_000017.10:g.4637831del , CM000679.1:g.4637831del GRCh37
NC_000017.9:g.4584580del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*23+50del MANE Select ENSP00000293778.7:n.*23+50del
ENST00000574412.6:c.*73del ENSP00000459592.2:n.*73del
ENST00000293778.10:c.*23+50del ENSP00000293778.6:n.*23+50del
ENST00000574412.5:c.*73del ENSP00000459592.1:n.*73del
ENST00000576153.5:n.579+50del
NM_001100812.1:c.*73del NP_001094282.1:n.*73del
NM_022059.3:c.*23+50del NP_071342.2:n.*23+50del
NM_022059.4:c.*23+50del NP_071342.2:n.*23+50del
NM_001100812.2:c.*73del NP_001094282.2:n.*73del
NM_001386809.1:c.*23+50del MANE Select NP_001373738.1:n.*23+50del