Canonical Allele Identifier: CA2244534095
Gene: CXCL16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734560T= , CM000679.2:g.4734560T= GRCh38
NC_000017.10:g.4637855T= , CM000679.1:g.4637855T= GRCh37
NC_000017.9:g.4584604T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*23+23A= MANE Select ENSP00000293778.7:n.*23+23A=
ENST00000574412.6:c.*46A= ENSP00000459592.2:n.*46A=
ENST00000293778.10:c.*23+23A= ENSP00000293778.6:n.*23+23A=
ENST00000574412.5:c.*46A= ENSP00000459592.1:n.*46A=
ENST00000576153.5:n.579+23A=
NM_001100812.1:c.*46A= NP_001094282.1:n.*46A=
NM_022059.3:c.*23+23A= NP_071342.2:n.*23+23A=
NM_022059.4:c.*23+23A= NP_071342.2:n.*23+23A=
NM_001100812.2:c.*46A= NP_001094282.2:n.*46A=
NM_001386809.1:c.*23+23A= MANE Select NP_001373738.1:n.*23+23A=
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