Canonical Allele Identifier: CA2244534092
Gene: CXCL16 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734559T= , CM000679.2:g.4734559T= GRCh38
NC_000017.10:g.4637854T= , CM000679.1:g.4637854T= GRCh37
NC_000017.9:g.4584603T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*23+24A= MANE Select ENSP00000293778.7:n.*23+24A=
ENST00000574412.6:c.*47A= ENSP00000459592.2:n.*47A=
ENST00000293778.10:c.*23+24A= ENSP00000293778.6:n.*23+24A=
ENST00000574412.5:c.*47A= ENSP00000459592.1:n.*47A=
ENST00000576153.5:n.579+24A=
NM_001100812.1:c.*47A= NP_001094282.1:n.*47A=
NM_022059.3:c.*23+24A= NP_071342.2:n.*23+24A=
NM_022059.4:c.*23+24A= NP_071342.2:n.*23+24A=
NM_001100812.2:c.*47A= NP_001094282.2:n.*47A=
NM_001386809.1:c.*23+24A= MANE Select NP_001373738.1:n.*23+24A=
Search 100 bp 5'
Search 100 bp 3'