Canonical Allele Identifier: CA2635550025
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734303-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734306del , CM000679.2:g.4734306del GRCh38
NC_000017.10:g.4637601del , CM000679.1:g.4637601del GRCh37
NC_000017.9:g.4584350del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*199del MANE Select ENSP00000293778.7:n.*199del
ENST00000574412.6:c.*302del ENSP00000459592.2:n.*302del
ENST00000293778.10:c.*199del ENSP00000293778.6:n.*199del
ENST00000574412.5:c.*302del ENSP00000459592.1:n.*302del
ENST00000576153.5:n.755del
NM_022059.3:c.*199del NP_071342.2:n.*199del
NM_022059.4:c.*199del NP_071342.2:n.*199del
NM_001386809.1:c.*199del MANE Select NP_001373738.1:n.*199del
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