Canonical Allele Identifier: CA2635549579

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734035-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734035_4734036insA , CM000679.2:g.4734035_4734036insA	GRCh38
NC_000017.10:g.4637330_4637331insA , CM000679.1:g.4637330_4637331insA	GRCh37
NC_000017.9:g.4584079_4584080insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*467_*468insT MANE Select	ENSP00000293778.7:n.*467_*468insT
ENST00000293778.10:c.*467_*468insT	ENSP00000293778.6:n.*467_*468insT
ENST00000576153.5:n.1023_1024insT
NM_022059.3:c.*467_*468insT	NP_071342.2:n.*467_*468insT
NM_022059.4:c.*467_*468insT	NP_071342.2:n.*467_*468insT
NM_001386809.1:c.*467_*468insT MANE Select	NP_001373738.1:n.*467_*468insT