Canonical Allele Identifier: CA2572347601

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734697_4734698insAGCTGGG , CM000679.2:g.4734697_4734698insAGCTGGG	GRCh38
NC_000017.10:g.4637992_4637993insAGCTGGG , CM000679.1:g.4637992_4637993insAGCTGGG	GRCh37
NC_000017.9:g.4584741_4584742insAGCTGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-46_719-45insCCCAGCT MANE Select	ENSP00000293778.7:n.719-46_719-45insCCCAGCT
ENST00000574412.6:c.719-46_719-45insCCCAGCT	ENSP00000459592.2:n.719-46_719-45insCCCAGCT
ENST00000293778.10:c.776-46_776-45insCCCAGCT	ENSP00000293778.6:n.776-46_776-45insCCCAGCT
ENST00000574412.5:c.776-46_776-45insCCCAGCT	ENSP00000459592.1:n.776-46_776-45insCCCAGCT
ENST00000575168.1:n.550-46_550-45insCCCAGCT
ENST00000576153.5:n.510-46_510-45insCCCAGCT
NM_001100812.1:c.776-46_776-45insCCCAGCT	NP_001094282.1:n.776-46_776-45insCCCAGCT
NM_022059.3:c.776-46_776-45insCCCAGCT	NP_071342.2:n.776-46_776-45insCCCAGCT
NM_022059.4:c.776-46_776-45insCCCAGCT	NP_071342.2:n.776-46_776-45insCCCAGCT
NM_001100812.2:c.719-46_719-45insCCCAGCT	NP_001094282.2:n.719-46_719-45insCCCAGCT
NM_001386809.1:c.719-46_719-45insCCCAGCT MANE Select	NP_001373738.1:n.719-46_719-45insCCCAGCT