Canonical Allele Identifier: CA2808290851
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734111_4734112insTGAGGC , CM000679.2:g.4734111_4734112insTGAGGC GRCh38
NC_000017.10:g.4637406_4637407insTGAGGC , CM000679.1:g.4637406_4637407insTGAGGC GRCh37
NC_000017.9:g.4584155_4584156insTGAGGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*396_*397insAGCCTC MANE Select ENSP00000293778.7:n.*396_*397insAGCCTC
ENST00000293778.10:c.*396_*397insAGCCTC ENSP00000293778.6:n.*396_*397insAGCCTC
ENST00000576153.5:n.952_953insAGCCTC
NM_022059.3:c.*396_*397insAGCCTC NP_071342.2:n.*396_*397insAGCCTC
NM_022059.4:c.*396_*397insAGCCTC NP_071342.2:n.*396_*397insAGCCTC
NM_001386809.1:c.*396_*397insAGCCTC MANE Select NP_001373738.1:n.*396_*397insAGCCTC