Canonical Allele Identifier: CA980962402
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916094200

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734566_4734567insCTTTATTACACTTT , CM000679.2:g.4734566_4734567insCTTTATTACACTTT GRCh38
NC_000017.10:g.4637861_4637862insCTTTATTACACTTT , CM000679.1:g.4637861_4637862insCTTTATTACACTTT GRCh37
NC_000017.9:g.4584610_4584611insCTTTATTACACTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*23+16_*23+17insAAAGTGTAATAAAG MANE Select ENSP00000293778.7:n.*23+16_*23+17insAAAGTGTAATAAAG
ENST00000574412.6:c.*39_*40insAAAGTGTAATAAAG ENSP00000459592.2:n.*39_*40insAAAGTGTAATAAAG
ENST00000293778.10:c.*23+16_*23+17insAAAGTGTAATAAAG ENSP00000293778.6:n.*23+16_*23+17insAAAGTGTAATAAAG
ENST00000574412.5:c.*39_*40insAAAGTGTAATAAAG ENSP00000459592.1:n.*39_*40insAAAGTGTAATAAAG
ENST00000576153.5:n.579+16_579+17insAAAGTGTAATAAAG
NM_001100812.1:c.*39_*40insAAAGTGTAATAAAG NP_001094282.1:n.*39_*40insAAAGTGTAATAAAG
NM_022059.3:c.*23+16_*23+17insAAAGTGTAATAAAG NP_071342.2:n.*23+16_*23+17insAAAGTGTAATAAAG
NM_022059.4:c.*23+16_*23+17insAAAGTGTAATAAAG NP_071342.2:n.*23+16_*23+17insAAAGTGTAATAAAG
NM_001100812.2:c.*39_*40insAAAGTGTAATAAAG NP_001094282.2:n.*39_*40insAAAGTGTAATAAAG
NM_001386809.1:c.*23+16_*23+17insAAAGTGTAATAAAG MANE Select NP_001373738.1:n.*23+16_*23+17insAAAGTGTAATAAAG