Canonical Allele Identifier: CA287188439

Gene: CXCL16

Linked Data

• dbSNP Id: rs779591660
• gnomAD v4: 17-4734458-CT-C
• MyVariant Identifiers: chr17:g.4637754del (hg19) ; chr17:g.4734459del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734459del , CM000679.2:g.4734459del	GRCh38
NC_000017.10:g.4637754del , CM000679.1:g.4637754del	GRCh37
NC_000017.9:g.4584503del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*44del MANE Select	ENSP00000293778.7:n.*44del
ENST00000574412.6:c.*147del	ENSP00000459592.2:n.*147del
ENST00000293778.10:c.*44del	ENSP00000293778.6:n.*44del
ENST00000574412.5:c.*147del	ENSP00000459592.1:n.*147del
ENST00000576153.5:n.600del
NM_022059.3:c.*44del	NP_071342.2:n.*44del
NM_022059.4:c.*44del	NP_071342.2:n.*44del
NM_001386809.1:c.*44del MANE Select	NP_001373738.1:n.*44del