Canonical Allele Identifier: CA2244533612
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734282_4734285delinsATTT , CM000679.2:g.4734282_4734285delinsATTT GRCh38
NC_000017.10:g.4637577_4637580delinsATTT , CM000679.1:g.4637577_4637580delinsATTT GRCh37
NC_000017.9:g.4584326_4584329delinsATTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*218_*221delinsAAAT MANE Select ENSP00000293778.7:n.*218_*221delinsAAAT
ENST00000293778.10:c.*218_*221delinsAAAT ENSP00000293778.6:n.*218_*221delinsAAAT
ENST00000576153.5:n.774_777delinsAAAT
NM_022059.3:c.*218_*221delinsAAAT NP_071342.2:n.*218_*221delinsAAAT
NM_022059.4:c.*218_*221delinsAAAT NP_071342.2:n.*218_*221delinsAAAT
NM_001386809.1:c.*218_*221delinsAAAT MANE Select NP_001373738.1:n.*218_*221delinsAAAT