Canonical Allele Identifier: CA2244533375
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916079254

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734121del , CM000679.2:g.4734121del GRCh38
NC_000017.10:g.4637416del , CM000679.1:g.4637416del GRCh37
NC_000017.9:g.4584165del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*382del MANE Select ENSP00000293778.7:n.*382del
ENST00000293778.10:c.*382del ENSP00000293778.6:n.*382del
ENST00000576153.5:n.938del
NM_022059.3:c.*382del NP_071342.2:n.*382del
NM_022059.4:c.*382del NP_071342.2:n.*382del
NM_001386809.1:c.*382del MANE Select NP_001373738.1:n.*382del