Canonical Allele Identifier: CA2635550071
Gene: CXCL16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734371_4734410dup , CM000679.2:g.4734371_4734410dup GRCh38
NC_000017.10:g.4637666_4637705dup , CM000679.1:g.4637666_4637705dup GRCh37
NC_000017.9:g.4584415_4584454dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*93_*132dup MANE Select ENSP00000293778.7:n.*93_*132dup
ENST00000574412.6:c.*196_*235dup ENSP00000459592.2:n.*196_*235dup
ENST00000293778.10:c.*93_*132dup ENSP00000293778.6:n.*93_*132dup
ENST00000574412.5:c.*196_*235dup ENSP00000459592.1:n.*196_*235dup
ENST00000576153.5:n.649_688dup
NM_022059.3:c.*93_*132dup NP_071342.2:n.*93_*132dup
NM_022059.4:c.*93_*132dup NP_071342.2:n.*93_*132dup
NM_001386809.1:c.*93_*132dup MANE Select NP_001373738.1:n.*93_*132dup