Canonical Allele Identifier: CA2509228957
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734034_4734035insG , CM000679.2:g.4734034_4734035insG GRCh38
NC_000017.10:g.4637329_4637330insG , CM000679.1:g.4637329_4637330insG GRCh37
NC_000017.9:g.4584078_4584079insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*468_*469insC MANE Select ENSP00000293778.7:n.*468_*469insC
ENST00000293778.10:c.*468_*469insC ENSP00000293778.6:n.*468_*469insC
ENST00000576153.5:n.1024_1025insC
NM_022059.3:c.*468_*469insC NP_071342.2:n.*468_*469insC
NM_022059.4:c.*468_*469insC NP_071342.2:n.*468_*469insC
NM_001386809.1:c.*468_*469insC MANE Select NP_001373738.1:n.*468_*469insC