Canonical Allele Identifier: CA2635550211
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734498_4734503del , CM000679.2:g.4734498_4734503del GRCh38
NC_000017.10:g.4637793_4637798del , CM000679.1:g.4637793_4637798del GRCh37
NC_000017.9:g.4584542_4584547del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-16_*24-11del MANE Select ENSP00000293778.7:n.*24-16_*24-11del
ENST00000574412.6:c.*111_*116del ENSP00000459592.2:n.*111_*116del
ENST00000293778.10:c.*24-16_*24-11del ENSP00000293778.6:n.*24-16_*24-11del
ENST00000574412.5:c.*111_*116del ENSP00000459592.1:n.*111_*116del
ENST00000576153.5:n.580-16_580-11del
NM_022059.3:c.*24-16_*24-11del NP_071342.2:n.*24-16_*24-11del
NM_022059.4:c.*24-16_*24-11del NP_071342.2:n.*24-16_*24-11del
NM_001386809.1:c.*24-16_*24-11del MANE Select NP_001373738.1:n.*24-16_*24-11del