Canonical Allele Identifier: CA2244533993
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916091890

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734500_4734503del , CM000679.2:g.4734500_4734503del GRCh38
NC_000017.10:g.4637795_4637798del , CM000679.1:g.4637795_4637798del GRCh37
NC_000017.9:g.4584544_4584547del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-22_*24-19del MANE Select ENSP00000293778.7:n.*24-22_*24-19del
ENST00000574412.6:c.*105_*108del ENSP00000459592.2:n.*105_*108del
ENST00000293778.10:c.*24-22_*24-19del ENSP00000293778.6:n.*24-22_*24-19del
ENST00000574412.5:c.*105_*108del ENSP00000459592.1:n.*105_*108del
ENST00000576153.5:n.580-22_580-19del
NM_022059.3:c.*24-22_*24-19del NP_071342.2:n.*24-22_*24-19del
NM_022059.4:c.*24-22_*24-19del NP_071342.2:n.*24-22_*24-19del
NM_001386809.1:c.*24-22_*24-19del MANE Select NP_001373738.1:n.*24-22_*24-19del