Canonical Allele Identifier: CA2635550303
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734563_4734571del , CM000679.2:g.4734563_4734571del GRCh38
NC_000017.10:g.4637858_4637866del , CM000679.1:g.4637858_4637866del GRCh37
NC_000017.9:g.4584607_4584615del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*23+12_*23+20del MANE Select ENSP00000293778.7:n.*23+12_*23+20del
ENST00000574412.6:c.*35_*43del ENSP00000459592.2:n.*35_*43del
ENST00000293778.10:c.*23+12_*23+20del ENSP00000293778.6:n.*23+12_*23+20del
ENST00000574412.5:c.*35_*43del ENSP00000459592.1:n.*35_*43del
ENST00000576153.5:n.579+12_579+20del
NM_001100812.1:c.*35_*43del NP_001094282.1:n.*35_*43del
NM_022059.3:c.*23+12_*23+20del NP_071342.2:n.*23+12_*23+20del
NM_022059.4:c.*23+12_*23+20del NP_071342.2:n.*23+12_*23+20del
NM_001100812.2:c.*35_*43del NP_001094282.2:n.*35_*43del
NM_001386809.1:c.*23+12_*23+20del MANE Select NP_001373738.1:n.*23+12_*23+20del