Canonical Allele Identifier: CA2635550057

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734342-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734344_4734345del , CM000679.2:g.4734344_4734345del	GRCh38
NC_000017.10:g.4637639_4637640del , CM000679.1:g.4637639_4637640del	GRCh37
NC_000017.9:g.4584388_4584389del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*159_*160del MANE Select	ENSP00000293778.7:n.*159_*160del
ENST00000574412.6:c.*262_*263del	ENSP00000459592.2:n.*262_*263del
ENST00000293778.10:c.*159_*160del	ENSP00000293778.6:n.*159_*160del
ENST00000574412.5:c.*262_*263del	ENSP00000459592.1:n.*262_*263del
ENST00000576153.5:n.715_716del
NM_022059.3:c.*159_*160del	NP_071342.2:n.*159_*160del
NM_022059.4:c.*159_*160del	NP_071342.2:n.*159_*160del
NM_001386809.1:c.*159_*160del MANE Select	NP_001373738.1:n.*159_*160del