Canonical Allele Identifier: CA2244533520
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734209_4734214delinsACAAAG , CM000679.2:g.4734209_4734214delinsACAAAG GRCh38
NC_000017.10:g.4637504_4637509delinsACAAAG , CM000679.1:g.4637504_4637509delinsACAAAG GRCh37
NC_000017.9:g.4584253_4584258delinsACAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*289_*294delinsCTTTGT MANE Select ENSP00000293778.7:n.*289_*294delinsCTTTGT
ENST00000293778.10:c.*289_*294delinsCTTTGT ENSP00000293778.6:n.*289_*294delinsCTTTGT
ENST00000576153.5:n.845_850delinsCTTTGT
NM_022059.3:c.*289_*294delinsCTTTGT NP_071342.2:n.*289_*294delinsCTTTGT
NM_022059.4:c.*289_*294delinsCTTTGT NP_071342.2:n.*289_*294delinsCTTTGT
NM_001386809.1:c.*289_*294delinsCTTTGT MANE Select NP_001373738.1:n.*289_*294delinsCTTTGT