Canonical Allele Identifier: CA2244533514
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734204_4734209delinsTCAAAA , CM000679.2:g.4734204_4734209delinsTCAAAA GRCh38
NC_000017.10:g.4637499_4637504delinsTCAAAA , CM000679.1:g.4637499_4637504delinsTCAAAA GRCh37
NC_000017.9:g.4584248_4584253delinsTCAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*294_*299delinsTTTTGA MANE Select ENSP00000293778.7:n.*294_*299delinsTTTTGA
ENST00000293778.10:c.*294_*299delinsTTTTGA ENSP00000293778.6:n.*294_*299delinsTTTTGA
ENST00000576153.5:n.850_855delinsTTTTGA
NM_022059.3:c.*294_*299delinsTTTTGA NP_071342.2:n.*294_*299delinsTTTTGA
NM_022059.4:c.*294_*299delinsTTTTGA NP_071342.2:n.*294_*299delinsTTTTGA
NM_001386809.1:c.*294_*299delinsTTTTGA MANE Select NP_001373738.1:n.*294_*299delinsTTTTGA