Canonical Allele Identifier: CA2244534191

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916097428
• gnomAD v4: 17-4734632-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734637_4734638dup , CM000679.2:g.4734637_4734638dup	GRCh38
NC_000017.10:g.4637932_4637933dup , CM000679.1:g.4637932_4637933dup	GRCh37
NC_000017.9:g.4584681_4584682dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.737_738dup MANE Select	ENSP00000293778.7:p.Pro247TyrfsTer?
ENST00000574412.6:c.737_738dup	ENSP00000459592.2:p.Pro247TyrfsTer?
ENST00000293778.10:c.794_795dup	ENSP00000293778.6:p.Pro266TyrfsTer?
ENST00000574412.5:c.794_795dup	ENSP00000459592.1:p.Pro266TyrfsTer?
ENST00000575168.1:n.568_569dup
ENST00000576153.5:n.528_529dup
NM_001100812.1:c.794_795dup	NP_001094282.1:p.Pro266TyrfsTer?
NM_022059.3:c.794_795dup	NP_071342.2:p.Pro266TyrfsTer?
NM_022059.4:c.794_795dup	NP_071342.2:p.Pro266TyrfsTer?
NM_001100812.2:c.737_738dup	NP_001094282.2:p.Pro247TyrfsTer?
NM_001386809.1:c.737_738dup MANE Select	NP_001373738.1:p.Pro247TyrfsTer?