Canonical Allele Identifier: CA2244534165
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734618G= , CM000679.2:g.4734618G= GRCh38
NC_000017.10:g.4637913G= , CM000679.1:g.4637913G= GRCh37
NC_000017.9:g.4584662G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.753C= MANE Select ENSP00000293778.7:p.Asp251=
ENST00000574412.6:c.753C= ENSP00000459592.2:p.Asp251=
ENST00000293778.10:c.810C= ENSP00000293778.6:p.Asp270=
ENST00000574412.5:c.810C= ENSP00000459592.1:p.Asp270=
ENST00000575168.1:n.584C=
ENST00000576153.5:n.544C=
NM_001100812.1:c.810C= NP_001094282.1:p.Asp270=
NM_022059.3:c.810C= NP_071342.2:p.Asp270=
NM_022059.4:c.810C= NP_071342.2:p.Asp270=
NM_001100812.2:c.753C= NP_001094282.2:p.Asp251=
NM_001386809.1:c.753C= MANE Select NP_001373738.1:p.Asp251=