Canonical Allele Identifier: CA2808290846
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734070_4734071insCTG , CM000679.2:g.4734070_4734071insCTG GRCh38
NC_000017.10:g.4637365_4637366insCTG , CM000679.1:g.4637365_4637366insCTG GRCh37
NC_000017.9:g.4584114_4584115insCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*434_*435insGCA MANE Select ENSP00000293778.7:n.*434_*435insGCA
ENST00000293778.10:c.*434_*435insGCA ENSP00000293778.6:n.*434_*435insGCA
ENST00000576153.5:n.990_991insGCA
NM_022059.3:c.*434_*435insGCA NP_071342.2:n.*434_*435insGCA
NM_022059.4:c.*434_*435insGCA NP_071342.2:n.*434_*435insGCA
NM_001386809.1:c.*434_*435insGCA MANE Select NP_001373738.1:n.*434_*435insGCA