Canonical Allele Identifier: CA980962097
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916082977

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734230_4734234del , CM000679.2:g.4734230_4734234del GRCh38
NC_000017.10:g.4637525_4637529del , CM000679.1:g.4637525_4637529del GRCh37
NC_000017.9:g.4584274_4584278del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*279_*283del MANE Select ENSP00000293778.7:n.*279_*283del
ENST00000293778.10:c.*279_*283del ENSP00000293778.6:n.*279_*283del
ENST00000576153.5:n.835_839del
NM_022059.3:c.*279_*283del NP_071342.2:n.*279_*283del
NM_022059.4:c.*279_*283del NP_071342.2:n.*279_*283del
NM_001386809.1:c.*279_*283del MANE Select NP_001373738.1:n.*279_*283del