Canonical Allele Identifier: CA2244533888
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734458_4734459delinsCT , CM000679.2:g.4734458_4734459delinsCT GRCh38
NC_000017.10:g.4637753_4637754delinsCT , CM000679.1:g.4637753_4637754delinsCT GRCh37
NC_000017.9:g.4584502_4584503delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*44_*45delinsAG MANE Select ENSP00000293778.7:n.*44_*45delinsAG
ENST00000574412.6:c.*147_*148delinsAG ENSP00000459592.2:n.*147_*148delinsAG
ENST00000293778.10:c.*44_*45delinsAG ENSP00000293778.6:n.*44_*45delinsAG
ENST00000574412.5:c.*147_*148delinsAG ENSP00000459592.1:n.*147_*148delinsAG
ENST00000576153.5:n.600_601delinsAG
NM_022059.3:c.*44_*45delinsAG NP_071342.2:n.*44_*45delinsAG
NM_022059.4:c.*44_*45delinsAG NP_071342.2:n.*44_*45delinsAG
NM_001386809.1:c.*44_*45delinsAG MANE Select NP_001373738.1:n.*44_*45delinsAG