Canonical Allele Identifier: CA2635550450

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734641-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734641_4734642insCC , CM000679.2:g.4734641_4734642insCC	GRCh38
NC_000017.10:g.4637936_4637937insCC , CM000679.1:g.4637936_4637937insCC	GRCh37
NC_000017.9:g.4584685_4584686insCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.729_730insGG MANE Select	ENSP00000293778.7:p.His244GlyfsTer?
ENST00000574412.6:c.729_730insGG	ENSP00000459592.2:p.His244GlyfsTer?
ENST00000293778.10:c.786_787insGG	ENSP00000293778.6:p.His263GlyfsTer?
ENST00000574412.5:c.786_787insGG	ENSP00000459592.1:p.His263GlyfsTer?
ENST00000575168.1:n.560_561insGG
ENST00000576153.5:n.520_521insGG
NM_001100812.1:c.786_787insGG	NP_001094282.1:p.His263GlyfsTer?
NM_022059.3:c.786_787insGG	NP_071342.2:p.His263GlyfsTer?
NM_022059.4:c.786_787insGG	NP_071342.2:p.His263GlyfsTer?
NM_001100812.2:c.729_730insGG	NP_001094282.2:p.His244GlyfsTer?
NM_001386809.1:c.729_730insGG MANE Select	NP_001373738.1:p.His244GlyfsTer?