Canonical Allele Identifier: CA2244533832
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734418A= , CM000679.2:g.4734418A= GRCh38
NC_000017.10:g.4637713A= , CM000679.1:g.4637713A= GRCh37
NC_000017.9:g.4584462A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*85T= MANE Select ENSP00000293778.7:n.*85T=
ENST00000574412.6:c.*188T= ENSP00000459592.2:n.*188T=
ENST00000293778.10:c.*85T= ENSP00000293778.6:n.*85T=
ENST00000574412.5:c.*188T= ENSP00000459592.1:n.*188T=
ENST00000576153.5:n.641T=
NM_022059.3:c.*85T= NP_071342.2:n.*85T=
NM_022059.4:c.*85T= NP_071342.2:n.*85T=
NM_001386809.1:c.*85T= MANE Select NP_001373738.1:n.*85T=