Canonical Allele Identifier: CA2635549961
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734228_4734229del , CM000679.2:g.4734228_4734229del GRCh38
NC_000017.10:g.4637523_4637524del , CM000679.1:g.4637523_4637524del GRCh37
NC_000017.9:g.4584272_4584273del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*276_*277del MANE Select ENSP00000293778.7:n.*276_*277del
ENST00000293778.10:c.*276_*277del ENSP00000293778.6:n.*276_*277del
ENST00000576153.5:n.832_833del
NM_022059.3:c.*276_*277del NP_071342.2:n.*276_*277del
NM_022059.4:c.*276_*277del NP_071342.2:n.*276_*277del
NM_001386809.1:c.*276_*277del MANE Select NP_001373738.1:n.*276_*277del