Canonical Allele Identifier: CA2635549581

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734036-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734036_4734037insT , CM000679.2:g.4734036_4734037insT	GRCh38
NC_000017.10:g.4637331_4637332insT , CM000679.1:g.4637331_4637332insT	GRCh37
NC_000017.9:g.4584080_4584081insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*466_*467insA MANE Select	ENSP00000293778.7:n.*466_*467insA
ENST00000293778.10:c.*466_*467insA	ENSP00000293778.6:n.*466_*467insA
ENST00000576153.5:n.1022_1023insA
NM_022059.3:c.*466_*467insA	NP_071342.2:n.*466_*467insA
NM_022059.4:c.*466_*467insA	NP_071342.2:n.*466_*467insA
NM_001386809.1:c.*466_*467insA MANE Select	NP_001373738.1:n.*466_*467insA