Canonical Allele Identifier: CA2635550207
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734494dup , CM000679.2:g.4734494dup GRCh38
NC_000017.10:g.4637789dup , CM000679.1:g.4637789dup GRCh37
NC_000017.9:g.4584538dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*24-10dup MANE Select ENSP00000293778.7:n.*24-10dup
ENST00000574412.6:c.*117dup ENSP00000459592.2:n.*117dup
ENST00000293778.10:c.*24-10dup ENSP00000293778.6:n.*24-10dup
ENST00000574412.5:c.*117dup ENSP00000459592.1:n.*117dup
ENST00000576153.5:n.580-10dup
NM_022059.3:c.*24-10dup NP_071342.2:n.*24-10dup
NM_022059.4:c.*24-10dup NP_071342.2:n.*24-10dup
NM_001386809.1:c.*24-10dup MANE Select NP_001373738.1:n.*24-10dup