Canonical Allele Identifier: CA2635550579
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734753_4734754del , CM000679.2:g.4734753_4734754del GRCh38
NC_000017.10:g.4638048_4638049del , CM000679.1:g.4638048_4638049del GRCh37
NC_000017.9:g.4584797_4584798del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.719-101_719-100del MANE Select ENSP00000293778.7:n.719-101_719-100del
ENST00000574412.6:c.719-101_719-100del ENSP00000459592.2:n.719-101_719-100del
ENST00000293778.10:c.776-101_776-100del ENSP00000293778.6:n.776-101_776-100del
ENST00000574412.5:c.776-101_776-100del ENSP00000459592.1:n.776-101_776-100del
ENST00000575168.1:n.550-101_550-100del
ENST00000576153.5:n.510-101_510-100del
NM_001100812.1:c.776-101_776-100del NP_001094282.1:n.776-101_776-100del
NM_022059.3:c.776-101_776-100del NP_071342.2:n.776-101_776-100del
NM_022059.4:c.776-101_776-100del NP_071342.2:n.776-101_776-100del
NM_001100812.2:c.719-101_719-100del NP_001094282.2:n.719-101_719-100del
NM_001386809.1:c.719-101_719-100del MANE Select NP_001373738.1:n.719-101_719-100del