Canonical Allele Identifier: CA2244533811
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734405A= , CM000679.2:g.4734405A= GRCh38
NC_000017.10:g.4637700A= , CM000679.1:g.4637700A= GRCh37
NC_000017.9:g.4584449A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*98T= MANE Select ENSP00000293778.7:n.*98T=
ENST00000574412.6:c.*201T= ENSP00000459592.2:n.*201T=
ENST00000293778.10:c.*98T= ENSP00000293778.6:n.*98T=
ENST00000574412.5:c.*201T= ENSP00000459592.1:n.*201T=
ENST00000576153.5:n.654T=
NM_022059.3:c.*98T= NP_071342.2:n.*98T=
NM_022059.4:c.*98T= NP_071342.2:n.*98T=
NM_001386809.1:c.*98T= MANE Select NP_001373738.1:n.*98T=