Canonical Allele Identifier: CA2244533821
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734414G= , CM000679.2:g.4734414G= GRCh38
NC_000017.10:g.4637709G= , CM000679.1:g.4637709G= GRCh37
NC_000017.9:g.4584458G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*89C= MANE Select ENSP00000293778.7:n.*89C=
ENST00000574412.6:c.*192C= ENSP00000459592.2:n.*192C=
ENST00000293778.10:c.*89C= ENSP00000293778.6:n.*89C=
ENST00000574412.5:c.*192C= ENSP00000459592.1:n.*192C=
ENST00000576153.5:n.645C=
NM_022059.3:c.*89C= NP_071342.2:n.*89C=
NM_022059.4:c.*89C= NP_071342.2:n.*89C=
NM_001386809.1:c.*89C= MANE Select NP_001373738.1:n.*89C=