Canonical Allele Identifier: CA980962217

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916089046
• gnomAD v3: 17-4734440-CAG-C
• gnomAD v4: 17-4734440-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734441_4734442del , CM000679.2:g.4734441_4734442del	GRCh38
NC_000017.10:g.4637736_4637737del , CM000679.1:g.4637736_4637737del	GRCh37
NC_000017.9:g.4584485_4584486del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*61_*62del MANE Select	ENSP00000293778.7:n.*61_*62del
ENST00000574412.6:c.*164_*165del	ENSP00000459592.2:n.*164_*165del
ENST00000293778.10:c.*61_*62del	ENSP00000293778.6:n.*61_*62del
ENST00000574412.5:c.*164_*165del	ENSP00000459592.1:n.*164_*165del
ENST00000576153.5:n.617_618del
NM_022059.3:c.*61_*62del	NP_071342.2:n.*61_*62del
NM_022059.4:c.*61_*62del	NP_071342.2:n.*61_*62del
NM_001386809.1:c.*61_*62del MANE Select	NP_001373738.1:n.*61_*62del