Canonical Allele Identifier: CA2635549851

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734147-A-AGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734148_4734149insCTG , CM000679.2:g.4734148_4734149insCTG	GRCh38
NC_000017.10:g.4637443_4637444insCTG , CM000679.1:g.4637443_4637444insCTG	GRCh37
NC_000017.9:g.4584192_4584193insCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*355_*356insAGC MANE Select	ENSP00000293778.7:n.*355_*356insAGC
ENST00000293778.10:c.*355_*356insAGC	ENSP00000293778.6:n.*355_*356insAGC
ENST00000576153.5:n.911_912insAGC
NM_022059.3:c.*355_*356insAGC	NP_071342.2:n.*355_*356insAGC
NM_022059.4:c.*355_*356insAGC	NP_071342.2:n.*355_*356insAGC
NM_001386809.1:c.*355_*356insAGC MANE Select	NP_001373738.1:n.*355_*356insAGC