Canonical Allele Identifier: CA2510779078

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734711_4734712insAGAGG , CM000679.2:g.4734711_4734712insAGAGG	GRCh38
NC_000017.10:g.4638006_4638007insAGAGG , CM000679.1:g.4638006_4638007insAGAGG	GRCh37
NC_000017.9:g.4584755_4584756insAGAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-60_719-59insCCTCT MANE Select	ENSP00000293778.7:n.719-60_719-59insCCTCT
ENST00000574412.6:c.719-60_719-59insCCTCT	ENSP00000459592.2:n.719-60_719-59insCCTCT
ENST00000293778.10:c.776-60_776-59insCCTCT	ENSP00000293778.6:n.776-60_776-59insCCTCT
ENST00000574412.5:c.776-60_776-59insCCTCT	ENSP00000459592.1:n.776-60_776-59insCCTCT
ENST00000575168.1:n.550-60_550-59insCCTCT
ENST00000576153.5:n.510-60_510-59insCCTCT
NM_001100812.1:c.776-60_776-59insCCTCT	NP_001094282.1:n.776-60_776-59insCCTCT
NM_022059.3:c.776-60_776-59insCCTCT	NP_071342.2:n.776-60_776-59insCCTCT
NM_022059.4:c.776-60_776-59insCCTCT	NP_071342.2:n.776-60_776-59insCCTCT
NM_001100812.2:c.719-60_719-59insCCTCT	NP_001094282.2:n.719-60_719-59insCCTCT
NM_001386809.1:c.719-60_719-59insCCTCT MANE Select	NP_001373738.1:n.719-60_719-59insCCTCT