Canonical Allele Identifier: CA2635549575
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734033_4734034insA , CM000679.2:g.4734033_4734034insA GRCh38
NC_000017.10:g.4637328_4637329insA , CM000679.1:g.4637328_4637329insA GRCh37
NC_000017.9:g.4584077_4584078insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*469_*470insT MANE Select ENSP00000293778.7:n.*469_*470insT
ENST00000293778.10:c.*469_*470insT ENSP00000293778.6:n.*469_*470insT
ENST00000576153.5:n.1025_1026insT
NM_022059.3:c.*469_*470insT NP_071342.2:n.*469_*470insT
NM_022059.4:c.*469_*470insT NP_071342.2:n.*469_*470insT
NM_001386809.1:c.*469_*470insT MANE Select NP_001373738.1:n.*469_*470insT