Canonical Allele Identifier: CA2244533538
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734219_4734224delinsGCAAAA , CM000679.2:g.4734219_4734224delinsGCAAAA GRCh38
NC_000017.10:g.4637514_4637519delinsGCAAAA , CM000679.1:g.4637514_4637519delinsGCAAAA GRCh37
NC_000017.9:g.4584263_4584268delinsGCAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*279_*284delinsTTTTGC MANE Select ENSP00000293778.7:n.*279_*284delinsTTTTGC
ENST00000293778.10:c.*279_*284delinsTTTTGC ENSP00000293778.6:n.*279_*284delinsTTTTGC
ENST00000576153.5:n.835_840delinsTTTTGC
NM_022059.3:c.*279_*284delinsTTTTGC NP_071342.2:n.*279_*284delinsTTTTGC
NM_022059.4:c.*279_*284delinsTTTTGC NP_071342.2:n.*279_*284delinsTTTTGC
NM_001386809.1:c.*279_*284delinsTTTTGC MANE Select NP_001373738.1:n.*279_*284delinsTTTTGC