Canonical Allele Identifier: CA980962039

Gene: CXCL16

Linked Data

• gnomAD v3: 17-4734106-G-GGCT
• gnomAD v4: 17-4734106-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734107_4734108insCTG , CM000679.2:g.4734107_4734108insCTG	GRCh38
NC_000017.10:g.4637402_4637403insCTG , CM000679.1:g.4637402_4637403insCTG	GRCh37
NC_000017.9:g.4584151_4584152insCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*396_*397insAGC MANE Select	ENSP00000293778.7:n.*396_*397insAGC
ENST00000293778.10:c.*396_*397insAGC	ENSP00000293778.6:n.*396_*397insAGC
ENST00000576153.5:n.952_953insAGC
NM_022059.3:c.*396_*397insAGC	NP_071342.2:n.*396_*397insAGC
NM_022059.4:c.*396_*397insAGC	NP_071342.2:n.*396_*397insAGC
NM_001386809.1:c.*396_*397insAGC MANE Select	NP_001373738.1:n.*396_*397insAGC