Canonical Allele Identifier: CA2244534394
Gene: CXCL16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734819C= , CM000679.2:g.4734819C= GRCh38
NC_000017.10:g.4638114C= , CM000679.1:g.4638114C= GRCh37
NC_000017.9:g.4584863C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.719-167G= MANE Select ENSP00000293778.7:n.719-167G=
ENST00000574412.6:c.719-167G= ENSP00000459592.2:n.719-167G=
ENST00000293778.10:c.776-167G= ENSP00000293778.6:n.776-167G=
ENST00000574412.5:c.776-167G= ENSP00000459592.1:n.776-167G=
ENST00000575168.1:n.550-167G=
ENST00000576153.5:n.510-167G=
NM_001100812.1:c.776-167G= NP_001094282.1:n.776-167G=
NM_022059.3:c.776-167G= NP_071342.2:n.776-167G=
NM_022059.4:c.776-167G= NP_071342.2:n.776-167G=
NM_001100812.2:c.719-167G= NP_001094282.2:n.719-167G=
NM_001386809.1:c.719-167G= MANE Select NP_001373738.1:n.719-167G=
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