Canonical Allele Identifier: CA2635550453

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734642-A-AGATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734642_4734643insGATCC , CM000679.2:g.4734642_4734643insGATCC	GRCh38
NC_000017.10:g.4637937_4637938insGATCC , CM000679.1:g.4637937_4637938insGATCC	GRCh37
NC_000017.9:g.4584686_4584687insGATCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.728_729insGGATC MANE Select	ENSP00000293778.7:p.His244AspfsTer?
ENST00000574412.6:c.728_729insGGATC	ENSP00000459592.2:p.His244AspfsTer?
ENST00000293778.10:c.785_786insGGATC	ENSP00000293778.6:p.His263AspfsTer?
ENST00000574412.5:c.785_786insGGATC	ENSP00000459592.1:p.His263AspfsTer?
ENST00000575168.1:n.559_560insGGATC
ENST00000576153.5:n.519_520insGGATC
NM_001100812.1:c.785_786insGGATC	NP_001094282.1:p.His263AspfsTer?
NM_022059.3:c.785_786insGGATC	NP_071342.2:p.His263AspfsTer?
NM_022059.4:c.785_786insGGATC	NP_071342.2:p.His263AspfsTer?
NM_001100812.2:c.728_729insGGATC	NP_001094282.2:p.His244AspfsTer?
NM_001386809.1:c.728_729insGGATC MANE Select	NP_001373738.1:p.His244AspfsTer?