Canonical Allele Identifier: CA2527845078
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734379-T-TC
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734379_4734380insC , CM000679.2:g.4734379_4734380insC GRCh38
NC_000017.10:g.4637674_4637675insC , CM000679.1:g.4637674_4637675insC GRCh37
NC_000017.9:g.4584423_4584424insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*123_*124insG MANE Select ENSP00000293778.7:n.*123_*124insG
ENST00000574412.6:c.*226_*227insG ENSP00000459592.2:n.*226_*227insG
ENST00000293778.10:c.*123_*124insG ENSP00000293778.6:n.*123_*124insG
ENST00000574412.5:c.*226_*227insG ENSP00000459592.1:n.*226_*227insG
ENST00000576153.5:n.679_680insG
NM_022059.3:c.*123_*124insG NP_071342.2:n.*123_*124insG
NM_022059.4:c.*123_*124insG NP_071342.2:n.*123_*124insG
NM_001386809.1:c.*123_*124insG MANE Select NP_001373738.1:n.*123_*124insG
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Search 100 bp 3'