Canonical Allele Identifier: CA2244533858
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734440_4734442delinsCAG , CM000679.2:g.4734440_4734442delinsCAG GRCh38
NC_000017.10:g.4637735_4637737delinsCAG , CM000679.1:g.4637735_4637737delinsCAG GRCh37
NC_000017.9:g.4584484_4584486delinsCAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*61_*63delinsCTG MANE Select ENSP00000293778.7:n.*61_*63delinsCTG
ENST00000574412.6:c.*164_*166delinsCTG ENSP00000459592.2:n.*164_*166delinsCTG
ENST00000293778.10:c.*61_*63delinsCTG ENSP00000293778.6:n.*61_*63delinsCTG
ENST00000574412.5:c.*164_*166delinsCTG ENSP00000459592.1:n.*164_*166delinsCTG
ENST00000576153.5:n.617_619delinsCTG
NM_022059.3:c.*61_*63delinsCTG NP_071342.2:n.*61_*63delinsCTG
NM_022059.4:c.*61_*63delinsCTG NP_071342.2:n.*61_*63delinsCTG
NM_001386809.1:c.*61_*63delinsCTG MANE Select NP_001373738.1:n.*61_*63delinsCTG