Canonical Allele Identifier: CA2635550520

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734700-GTGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734703_4734706del , CM000679.2:g.4734703_4734706del	GRCh38
NC_000017.10:g.4637998_4638001del , CM000679.1:g.4637998_4638001del	GRCh37
NC_000017.9:g.4584747_4584750del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-52_719-49del MANE Select	ENSP00000293778.7:n.719-52_719-49del
ENST00000574412.6:c.719-52_719-49del	ENSP00000459592.2:n.719-52_719-49del
ENST00000293778.10:c.776-52_776-49del	ENSP00000293778.6:n.776-52_776-49del
ENST00000574412.5:c.776-52_776-49del	ENSP00000459592.1:n.776-52_776-49del
ENST00000575168.1:n.550-52_550-49del
ENST00000576153.5:n.510-52_510-49del
NM_001100812.1:c.776-52_776-49del	NP_001094282.1:n.776-52_776-49del
NM_022059.3:c.776-52_776-49del	NP_071342.2:n.776-52_776-49del
NM_022059.4:c.776-52_776-49del	NP_071342.2:n.776-52_776-49del
NM_001100812.2:c.719-52_719-49del	NP_001094282.2:n.719-52_719-49del
NM_001386809.1:c.719-52_719-49del MANE Select	NP_001373738.1:n.719-52_719-49del