Canonical Allele Identifier: CA2244534364
Gene: CXCL16 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734772G= , CM000679.2:g.4734772G= GRCh38
NC_000017.10:g.4638067G= , CM000679.1:g.4638067G= GRCh37
NC_000017.9:g.4584816G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.719-120C= MANE Select ENSP00000293778.7:n.719-120C=
ENST00000574412.6:c.719-120C= ENSP00000459592.2:n.719-120C=
ENST00000293778.10:c.776-120C= ENSP00000293778.6:n.776-120C=
ENST00000574412.5:c.776-120C= ENSP00000459592.1:n.776-120C=
ENST00000575168.1:n.550-120C=
ENST00000576153.5:n.510-120C=
NM_001100812.1:c.776-120C= NP_001094282.1:n.776-120C=
NM_022059.3:c.776-120C= NP_071342.2:n.776-120C=
NM_022059.4:c.776-120C= NP_071342.2:n.776-120C=
NM_001100812.2:c.719-120C= NP_001094282.2:n.719-120C=
NM_001386809.1:c.719-120C= MANE Select NP_001373738.1:n.719-120C=
Search 100 bp 5'
Search 100 bp 3'