Canonical Allele Identifier: CA2244533862
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734440_4734443delinsCAGG , CM000679.2:g.4734440_4734443delinsCAGG GRCh38
NC_000017.10:g.4637735_4637738delinsCAGG , CM000679.1:g.4637735_4637738delinsCAGG GRCh37
NC_000017.9:g.4584484_4584487delinsCAGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*60_*63delinsCCTG MANE Select ENSP00000293778.7:n.*60_*63delinsCCTG
ENST00000574412.6:c.*163_*166delinsCCTG ENSP00000459592.2:n.*163_*166delinsCCTG
ENST00000293778.10:c.*60_*63delinsCCTG ENSP00000293778.6:n.*60_*63delinsCCTG
ENST00000574412.5:c.*163_*166delinsCCTG ENSP00000459592.1:n.*163_*166delinsCCTG
ENST00000576153.5:n.616_619delinsCCTG
NM_022059.3:c.*60_*63delinsCCTG NP_071342.2:n.*60_*63delinsCCTG
NM_022059.4:c.*60_*63delinsCCTG NP_071342.2:n.*60_*63delinsCCTG
NM_001386809.1:c.*60_*63delinsCCTG MANE Select NP_001373738.1:n.*60_*63delinsCCTG