Canonical Allele Identifier: CA2244534041
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734525T= , CM000679.2:g.4734525T= GRCh38
NC_000017.10:g.4637820T= , CM000679.1:g.4637820T= GRCh37
NC_000017.9:g.4584569T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*24-46A= MANE Select ENSP00000293778.7:n.*24-46A=
ENST00000574412.6:c.*81A= ENSP00000459592.2:n.*81A=
ENST00000293778.10:c.*24-46A= ENSP00000293778.6:n.*24-46A=
ENST00000574412.5:c.*81A= ENSP00000459592.1:n.*81A=
ENST00000576153.5:n.580-46A=
NM_001100812.1:c.*81A= NP_001094282.1:n.*81A=
NM_022059.3:c.*24-46A= NP_071342.2:n.*24-46A=
NM_022059.4:c.*24-46A= NP_071342.2:n.*24-46A=
NM_001100812.2:c.*81A= NP_001094282.2:n.*81A=
NM_001386809.1:c.*24-46A= MANE Select NP_001373738.1:n.*24-46A=