Canonical Allele Identifier: CA980962408

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916094375
• gnomAD v3: 17-4734570-AGC-A
• gnomAD v4: 17-4734570-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734571_4734572del , CM000679.2:g.4734571_4734572del	GRCh38
NC_000017.10:g.4637866_4637867del , CM000679.1:g.4637866_4637867del	GRCh37
NC_000017.9:g.4584615_4584616del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+11_*23+12del MANE Select	ENSP00000293778.7:n.*23+11_*23+12del
ENST00000574412.6:c.*34_*35del	ENSP00000459592.2:n.*34_*35del
ENST00000293778.10:c.*23+11_*23+12del	ENSP00000293778.6:n.*23+11_*23+12del
ENST00000574412.5:c.*34_*35del	ENSP00000459592.1:n.*34_*35del
ENST00000576153.5:n.579+11_579+12del
NM_001100812.1:c.*34_*35del	NP_001094282.1:n.*34_*35del
NM_022059.3:c.*23+11_*23+12del	NP_071342.2:n.*23+11_*23+12del
NM_022059.4:c.*23+11_*23+12del	NP_071342.2:n.*23+11_*23+12del
NM_001100812.2:c.*34_*35del	NP_001094282.2:n.*34_*35del
NM_001386809.1:c.*23+11_*23+12del MANE Select	NP_001373738.1:n.*23+11_*23+12del