Canonical Allele Identifier: CA2808290855
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734130_4734131del , CM000679.2:g.4734130_4734131del GRCh38
NC_000017.10:g.4637425_4637426del , CM000679.1:g.4637425_4637426del GRCh37
NC_000017.9:g.4584174_4584175del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*372_*373del MANE Select ENSP00000293778.7:n.*372_*373del
ENST00000293778.10:c.*372_*373del ENSP00000293778.6:n.*372_*373del
ENST00000576153.5:n.928_929del
NM_022059.3:c.*372_*373del NP_071342.2:n.*372_*373del
NM_022059.4:c.*372_*373del NP_071342.2:n.*372_*373del
NM_001386809.1:c.*372_*373del MANE Select NP_001373738.1:n.*372_*373del