Canonical Allele Identifier: CA2244534009
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734507T= , CM000679.2:g.4734507T= GRCh38
NC_000017.10:g.4637802T= , CM000679.1:g.4637802T= GRCh37
NC_000017.9:g.4584551T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-28A= MANE Select ENSP00000293778.7:n.*24-28A=
ENST00000574412.6:c.*99A= ENSP00000459592.2:n.*99A=
ENST00000293778.10:c.*24-28A= ENSP00000293778.6:n.*24-28A=
ENST00000574412.5:c.*99A= ENSP00000459592.1:n.*99A=
ENST00000576153.5:n.580-28A=
NM_022059.3:c.*24-28A= NP_071342.2:n.*24-28A=
NM_022059.4:c.*24-28A= NP_071342.2:n.*24-28A=
NM_001386809.1:c.*24-28A= MANE Select NP_001373738.1:n.*24-28A=