Canonical Allele Identifier: CA2576133304
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734587dup , CM000679.2:g.4734587dup GRCh38
NC_000017.10:g.4637882dup , CM000679.1:g.4637882dup GRCh37
NC_000017.9:g.4584631dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*19dup MANE Select ENSP00000293778.7:n.*19dup
ENST00000574412.6:c.*19dup ENSP00000459592.2:n.*19dup
ENST00000293778.10:c.*19dup ENSP00000293778.6:n.*19dup
ENST00000574412.5:c.*19dup ENSP00000459592.1:n.*19dup
ENST00000575168.1:n.615dup
ENST00000576153.5:n.575dup
NM_001100812.1:c.*19dup NP_001094282.1:n.*19dup
NM_022059.3:c.*19dup NP_071342.2:n.*19dup
NM_022059.4:c.*19dup NP_071342.2:n.*19dup
NM_001100812.2:c.*19dup NP_001094282.2:n.*19dup
NM_001386809.1:c.*19dup MANE Select NP_001373738.1:n.*19dup