Canonical Allele Identifier: CA2244533259
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734037_4734039delinsGTC , CM000679.2:g.4734037_4734039delinsGTC GRCh38
NC_000017.10:g.4637332_4637334delinsGTC , CM000679.1:g.4637332_4637334delinsGTC GRCh37
NC_000017.9:g.4584081_4584083delinsGTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*464_*466delinsGAC MANE Select ENSP00000293778.7:n.*464_*466delinsGAC
ENST00000293778.10:c.*464_*466delinsGAC ENSP00000293778.6:n.*464_*466delinsGAC
ENST00000576153.5:n.1020_1022delinsGAC
NM_022059.3:c.*464_*466delinsGAC NP_071342.2:n.*464_*466delinsGAC
NM_022059.4:c.*464_*466delinsGAC NP_071342.2:n.*464_*466delinsGAC
NM_001386809.1:c.*464_*466delinsGAC MANE Select NP_001373738.1:n.*464_*466delinsGAC