Canonical Allele Identifier: CA2244534157
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734614T= , CM000679.2:g.4734614T= GRCh38
NC_000017.10:g.4637909T= , CM000679.1:g.4637909T= GRCh37
NC_000017.9:g.4584658T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.757A= MANE Select ENSP00000293778.7:p.Asn253=
ENST00000574412.6:c.757A= ENSP00000459592.2:p.Asn253=
ENST00000293778.10:c.814A= ENSP00000293778.6:p.Asn272=
ENST00000574412.5:c.814A= ENSP00000459592.1:p.Asn272=
ENST00000575168.1:n.588A=
ENST00000576153.5:n.548A=
NM_001100812.1:c.814A= NP_001094282.1:p.Asn272=
NM_022059.3:c.814A= NP_071342.2:p.Asn272=
NM_022059.4:c.814A= NP_071342.2:p.Asn272=
NM_001100812.2:c.757A= NP_001094282.2:p.Asn253=
NM_001386809.1:c.757A= MANE Select NP_001373738.1:p.Asn253=