Canonical Allele Identifier: CA2244534050

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734531_4734533delinsCAG , CM000679.2:g.4734531_4734533delinsCAG	GRCh38
NC_000017.10:g.4637826_4637828delinsCAG , CM000679.1:g.4637826_4637828delinsCAG	GRCh37
NC_000017.9:g.4584575_4584577delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+50_*24-52delinsCTG MANE Select	ENSP00000293778.7:n.*23+50_*24-52delinsCTG
ENST00000574412.6:c.*73_*75delinsCTG	ENSP00000459592.2:n.*73_*75delinsCTG
ENST00000293778.10:c.*23+50_*24-52delinsCTG	ENSP00000293778.6:n.*23+50_*24-52delinsCTG
ENST00000574412.5:c.*73_*75delinsCTG	ENSP00000459592.1:n.*73_*75delinsCTG
ENST00000576153.5:n.579+50_580-52delinsCTG
NM_001100812.1:c.*73_*75delinsCTG	NP_001094282.1:n.*73_*75delinsCTG
NM_022059.3:c.*23+50_*24-52delinsCTG	NP_071342.2:n.*23+50_*24-52delinsCTG
NM_022059.4:c.*23+50_*24-52delinsCTG	NP_071342.2:n.*23+50_*24-52delinsCTG
NM_001100812.2:c.*73_*75delinsCTG	NP_001094282.2:n.*73_*75delinsCTG
NM_001386809.1:c.*23+50_*24-52delinsCTG MANE Select	NP_001373738.1:n.*23+50_*24-52delinsCTG