Canonical Allele Identifier: CA2244534332

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734746_4734747delinsCA , CM000679.2:g.4734746_4734747delinsCA	GRCh38
NC_000017.10:g.4638041_4638042delinsCA , CM000679.1:g.4638041_4638042delinsCA	GRCh37
NC_000017.9:g.4584790_4584791delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-95_719-94delinsTG MANE Select	ENSP00000293778.7:n.719-95_719-94delinsTG
ENST00000574412.6:c.719-95_719-94delinsTG	ENSP00000459592.2:n.719-95_719-94delinsTG
ENST00000293778.10:c.776-95_776-94delinsTG	ENSP00000293778.6:n.776-95_776-94delinsTG
ENST00000574412.5:c.776-95_776-94delinsTG	ENSP00000459592.1:n.776-95_776-94delinsTG
ENST00000575168.1:n.550-95_550-94delinsTG
ENST00000576153.5:n.510-95_510-94delinsTG
NM_001100812.1:c.776-95_776-94delinsTG	NP_001094282.1:n.776-95_776-94delinsTG
NM_022059.3:c.776-95_776-94delinsTG	NP_071342.2:n.776-95_776-94delinsTG
NM_022059.4:c.776-95_776-94delinsTG	NP_071342.2:n.776-95_776-94delinsTG
NM_001100812.2:c.719-95_719-94delinsTG	NP_001094282.2:n.719-95_719-94delinsTG
NM_001386809.1:c.719-95_719-94delinsTG MANE Select	NP_001373738.1:n.719-95_719-94delinsTG