Canonical Allele Identifier: CA2635549724
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734099_4734100insAGC , CM000679.2:g.4734099_4734100insAGC GRCh38
NC_000017.10:g.4637394_4637395insAGC , CM000679.1:g.4637394_4637395insAGC GRCh37
NC_000017.9:g.4584143_4584144insAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*404_*405insCTG MANE Select ENSP00000293778.7:n.*404_*405insCTG
ENST00000293778.10:c.*404_*405insCTG ENSP00000293778.6:n.*404_*405insCTG
ENST00000576153.5:n.960_961insCTG
NM_022059.3:c.*404_*405insCTG NP_071342.2:n.*404_*405insCTG
NM_022059.4:c.*404_*405insCTG NP_071342.2:n.*404_*405insCTG
NM_001386809.1:c.*404_*405insCTG MANE Select NP_001373738.1:n.*404_*405insCTG