Canonical Allele Identifier: CA2635550487
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734675_4734678del , CM000679.2:g.4734675_4734678del GRCh38
NC_000017.10:g.4637970_4637973del , CM000679.1:g.4637970_4637973del GRCh37
NC_000017.9:g.4584719_4584722del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.719-24_719-21del MANE Select ENSP00000293778.7:n.719-24_719-21del
ENST00000574412.6:c.719-24_719-21del ENSP00000459592.2:n.719-24_719-21del
ENST00000293778.10:c.776-24_776-21del ENSP00000293778.6:n.776-24_776-21del
ENST00000574412.5:c.776-24_776-21del ENSP00000459592.1:n.776-24_776-21del
ENST00000575168.1:n.550-24_550-21del
ENST00000576153.5:n.510-24_510-21del
NM_001100812.1:c.776-24_776-21del NP_001094282.1:n.776-24_776-21del
NM_022059.3:c.776-24_776-21del NP_071342.2:n.776-24_776-21del
NM_022059.4:c.776-24_776-21del NP_071342.2:n.776-24_776-21del
NM_001100812.2:c.719-24_719-21del NP_001094282.2:n.719-24_719-21del
NM_001386809.1:c.719-24_719-21del MANE Select NP_001373738.1:n.719-24_719-21del