Canonical Allele Identifier: CA2635550629

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734787-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734790_4734791del , CM000679.2:g.4734790_4734791del	GRCh38
NC_000017.10:g.4638085_4638086del , CM000679.1:g.4638085_4638086del	GRCh37
NC_000017.9:g.4584834_4584835del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-137_719-136del MANE Select	ENSP00000293778.7:n.719-137_719-136del
ENST00000574412.6:c.719-137_719-136del	ENSP00000459592.2:n.719-137_719-136del
ENST00000293778.10:c.776-137_776-136del	ENSP00000293778.6:n.776-137_776-136del
ENST00000574412.5:c.776-137_776-136del	ENSP00000459592.1:n.776-137_776-136del
ENST00000575168.1:n.550-137_550-136del
ENST00000576153.5:n.510-137_510-136del
NM_001100812.1:c.776-137_776-136del	NP_001094282.1:n.776-137_776-136del
NM_022059.3:c.776-137_776-136del	NP_071342.2:n.776-137_776-136del
NM_022059.4:c.776-137_776-136del	NP_071342.2:n.776-137_776-136del
NM_001100812.2:c.719-137_719-136del	NP_001094282.2:n.719-137_719-136del
NM_001386809.1:c.719-137_719-136del MANE Select	NP_001373738.1:n.719-137_719-136del