Canonical Allele Identifier: CA2635550020
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734291del , CM000679.2:g.4734291del GRCh38
NC_000017.10:g.4637586del , CM000679.1:g.4637586del GRCh37
NC_000017.9:g.4584335del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*212del MANE Select ENSP00000293778.7:n.*212del
ENST00000574412.6:c.*315del ENSP00000459592.2:n.*315del
ENST00000293778.10:c.*212del ENSP00000293778.6:n.*212del
ENST00000574412.5:c.*315del ENSP00000459592.1:n.*315del
ENST00000576153.5:n.768del
NM_022059.3:c.*212del NP_071342.2:n.*212del
NM_022059.4:c.*212del NP_071342.2:n.*212del
NM_001386809.1:c.*212del MANE Select NP_001373738.1:n.*212del