Canonical Allele Identifier: CA397281525
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734637T>A , CM000679.2:g.4734637T>A GRCh38
NC_000017.10:g.4637932T>A , CM000679.1:g.4637932T>A GRCh37
NC_000017.9:g.4584681T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.734A>T MANE Select ENSP00000293778.7:p.Tyr245Phe
ENST00000574412.6:c.734A>T ENSP00000459592.2:p.Tyr245Phe
ENST00000293778.10:c.791A>T ENSP00000293778.6:p.Tyr264Phe
ENST00000574412.5:c.791A>T ENSP00000459592.1:p.Tyr264Phe
ENST00000575168.1:n.565A>T
ENST00000576153.5:n.525A>T
NM_001100812.1:c.791A>T NP_001094282.1:p.Tyr264Phe
NM_022059.3:c.791A>T NP_071342.2:p.Tyr264Phe
NM_022059.4:c.791A>T NP_071342.2:p.Tyr264Phe
NM_001100812.2:c.734A>T NP_001094282.2:p.Tyr245Phe
NM_001386809.1:c.734A>T MANE Select NP_001373738.1:p.Tyr245Phe