Canonical Allele Identifier: CA2569542984
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734392-C-CG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734392_4734393insG , CM000679.2:g.4734392_4734393insG GRCh38
NC_000017.10:g.4637687_4637688insG , CM000679.1:g.4637687_4637688insG GRCh37
NC_000017.9:g.4584436_4584437insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*110_*111insC MANE Select ENSP00000293778.7:n.*110_*111insC
ENST00000574412.6:c.*213_*214insC ENSP00000459592.2:n.*213_*214insC
ENST00000293778.10:c.*110_*111insC ENSP00000293778.6:n.*110_*111insC
ENST00000574412.5:c.*213_*214insC ENSP00000459592.1:n.*213_*214insC
ENST00000576153.5:n.666_667insC
NM_022059.3:c.*110_*111insC NP_071342.2:n.*110_*111insC
NM_022059.4:c.*110_*111insC NP_071342.2:n.*110_*111insC
NM_001386809.1:c.*110_*111insC MANE Select NP_001373738.1:n.*110_*111insC
Search 100 bp 5'
Search 100 bp 3'