Canonical Allele Identifier: CA2244533962
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916091496

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734491_4734494del , CM000679.2:g.4734491_4734494del GRCh38
NC_000017.10:g.4637786_4637789del , CM000679.1:g.4637786_4637789del GRCh37
NC_000017.9:g.4584535_4584538del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*24-13_*24-10del MANE Select ENSP00000293778.7:n.*24-13_*24-10del
ENST00000574412.6:c.*114_*117del ENSP00000459592.2:n.*114_*117del
ENST00000293778.10:c.*24-13_*24-10del ENSP00000293778.6:n.*24-13_*24-10del
ENST00000574412.5:c.*114_*117del ENSP00000459592.1:n.*114_*117del
ENST00000576153.5:n.580-13_580-10del
NM_022059.3:c.*24-13_*24-10del NP_071342.2:n.*24-13_*24-10del
NM_022059.4:c.*24-13_*24-10del NP_071342.2:n.*24-13_*24-10del
NM_001386809.1:c.*24-13_*24-10del MANE Select NP_001373738.1:n.*24-13_*24-10del