Canonical Allele Identifier: CA772507113

Gene: CXCL16

Linked Data

• dbSNP Id: rs1477247809
• gnomAD v3: 17-4734531-CAG-C
• gnomAD v4: 17-4734531-CAG-C
• MyVariant Identifiers: chr17:g.4637827_4637828del (hg19) ; chr17:g.4734532_4734533del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734532_4734533del , CM000679.2:g.4734532_4734533del	GRCh38
NC_000017.10:g.4637827_4637828del , CM000679.1:g.4637827_4637828del	GRCh37
NC_000017.9:g.4584576_4584577del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+50_*23+51del MANE Select	ENSP00000293778.7:n.*23+50_*23+51del
ENST00000574412.6:c.*73_*74del	ENSP00000459592.2:n.*73_*74del
ENST00000293778.10:c.*23+50_*23+51del	ENSP00000293778.6:n.*23+50_*23+51del
ENST00000574412.5:c.*73_*74del	ENSP00000459592.1:n.*73_*74del
ENST00000576153.5:n.579+50_579+51del
NM_001100812.1:c.*73_*74del	NP_001094282.1:n.*73_*74del
NM_022059.3:c.*23+50_*23+51del	NP_071342.2:n.*23+50_*23+51del
NM_022059.4:c.*23+50_*23+51del	NP_071342.2:n.*23+50_*23+51del
NM_001100812.2:c.*73_*74del	NP_001094282.2:n.*73_*74del
NM_001386809.1:c.*23+50_*23+51del MANE Select	NP_001373738.1:n.*23+50_*23+51del