Canonical Allele Identifier: CA772507112

Gene: CXCL16

Linked Data

• dbSNP Id: rs1168068165
• gnomAD v3: 17-4734528-TGTC-T
• gnomAD v4: 17-4734528-TGTC-T
• MyVariant Identifiers: chr17:g.4637824_4637826del (hg19) ; chr17:g.4734529_4734531del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734529_4734531del , CM000679.2:g.4734529_4734531del	GRCh38
NC_000017.10:g.4637824_4637826del , CM000679.1:g.4637824_4637826del	GRCh37
NC_000017.9:g.4584573_4584575del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*24-52_*24-50del MANE Select	ENSP00000293778.7:n.*24-52_*24-50del
ENST00000574412.6:c.*75_*77del	ENSP00000459592.2:n.*75_*77del
ENST00000293778.10:c.*24-52_*24-50del	ENSP00000293778.6:n.*24-52_*24-50del
ENST00000574412.5:c.*75_*77del	ENSP00000459592.1:n.*75_*77del
ENST00000576153.5:n.580-52_580-50del
NM_001100812.1:c.*75_*77del	NP_001094282.1:n.*75_*77del
NM_022059.3:c.*24-52_*24-50del	NP_071342.2:n.*24-52_*24-50del
NM_022059.4:c.*24-52_*24-50del	NP_071342.2:n.*24-52_*24-50del
NM_001100812.2:c.*75_*77del	NP_001094282.2:n.*75_*77del
NM_001386809.1:c.*24-52_*24-50del MANE Select	NP_001373738.1:n.*24-52_*24-50del