Canonical Allele Identifier: CA980962125

Gene: CXCL16

Linked Data

• dbSNP Id: rs1773229490
• gnomAD v3: 17-4734309-A-AG
• gnomAD v4: 17-4734309-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734313dup , CM000679.2:g.4734313dup	GRCh38
NC_000017.10:g.4637608dup , CM000679.1:g.4637608dup	GRCh37
NC_000017.9:g.4584357dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*193dup MANE Select	ENSP00000293778.7:n.*193dup
ENST00000574412.6:c.*296dup	ENSP00000459592.2:n.*296dup
ENST00000293778.10:c.*193dup	ENSP00000293778.6:n.*193dup
ENST00000574412.5:c.*296dup	ENSP00000459592.1:n.*296dup
ENST00000576153.5:n.749dup
NM_022059.3:c.*193dup	NP_071342.2:n.*193dup
NM_022059.4:c.*193dup	NP_071342.2:n.*193dup
NM_001386809.1:c.*193dup MANE Select	NP_001373738.1:n.*193dup