Canonical Allele Identifier: CA980962226

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916089683
• gnomAD v4: 17-4734450-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734451dup , CM000679.2:g.4734451dup	GRCh38
NC_000017.10:g.4637746dup , CM000679.1:g.4637746dup	GRCh37
NC_000017.9:g.4584495dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*52dup MANE Select	ENSP00000293778.7:n.*52dup
ENST00000574412.6:c.*155dup	ENSP00000459592.2:n.*155dup
ENST00000293778.10:c.*52dup	ENSP00000293778.6:n.*52dup
ENST00000574412.5:c.*155dup	ENSP00000459592.1:n.*155dup
ENST00000576153.5:n.608dup
NM_022059.3:c.*52dup	NP_071342.2:n.*52dup
NM_022059.4:c.*52dup	NP_071342.2:n.*52dup
NM_001386809.1:c.*52dup MANE Select	NP_001373738.1:n.*52dup