Canonical Allele Identifier: CA2244533481
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916081436

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734190_4734191del , CM000679.2:g.4734190_4734191del GRCh38
NC_000017.10:g.4637485_4637486del , CM000679.1:g.4637485_4637486del GRCh37
NC_000017.9:g.4584234_4584235del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*314_*315del MANE Select ENSP00000293778.7:n.*314_*315del
ENST00000293778.10:c.*314_*315del ENSP00000293778.6:n.*314_*315del
ENST00000576153.5:n.870_871del
NM_022059.3:c.*314_*315del NP_071342.2:n.*314_*315del
NM_022059.4:c.*314_*315del NP_071342.2:n.*314_*315del
NM_001386809.1:c.*314_*315del MANE Select NP_001373738.1:n.*314_*315del