Canonical Allele Identifier: CA397281402
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734613T>A , CM000679.2:g.4734613T>A GRCh38
NC_000017.10:g.4637908T>A , CM000679.1:g.4637908T>A GRCh37
NC_000017.9:g.4584657T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.758A>T MANE Select ENSP00000293778.7:p.Asn253Ile
ENST00000574412.6:c.758A>T ENSP00000459592.2:p.Asn253Ile
ENST00000293778.10:c.815A>T ENSP00000293778.6:p.Asn272Ile
ENST00000574412.5:c.815A>T ENSP00000459592.1:p.Asn272Ile
ENST00000575168.1:n.589A>T
ENST00000576153.5:n.549A>T
NM_001100812.1:c.815A>T NP_001094282.1:p.Asn272Ile
NM_022059.3:c.815A>T NP_071342.2:p.Asn272Ile
NM_022059.4:c.815A>T NP_071342.2:p.Asn272Ile
NM_001100812.2:c.758A>T NP_001094282.2:p.Asn253Ile
NM_001386809.1:c.758A>T MANE Select NP_001373738.1:p.Asn253Ile