Canonical Allele Identifier: CA397281399
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734612A>T , CM000679.2:g.4734612A>T GRCh38
NC_000017.10:g.4637907A>T , CM000679.1:g.4637907A>T GRCh37
NC_000017.9:g.4584656A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.759T>A MANE Select ENSP00000293778.7:p.Asn253Lys
ENST00000574412.6:c.759T>A ENSP00000459592.2:p.Asn253Lys
ENST00000293778.10:c.816T>A ENSP00000293778.6:p.Asn272Lys
ENST00000574412.5:c.816T>A ENSP00000459592.1:p.Asn272Lys
ENST00000575168.1:n.590T>A
ENST00000576153.5:n.550T>A
NM_001100812.1:c.816T>A NP_001094282.1:p.Asn272Lys
NM_022059.3:c.816T>A NP_071342.2:p.Asn272Lys
NM_022059.4:c.816T>A NP_071342.2:p.Asn272Lys
NM_001100812.2:c.759T>A NP_001094282.2:p.Asn253Lys
NM_001386809.1:c.759T>A MANE Select NP_001373738.1:p.Asn253Lys