Canonical Allele Identifier: CA397281600

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734646-G-C
• MyVariant Identifiers: chr17:g.4637941G>C (hg19) ; chr17:g.4734646G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734646G>C , CM000679.2:g.4734646G>C	GRCh38
NC_000017.10:g.4637941G>C , CM000679.1:g.4637941G>C	GRCh37
NC_000017.9:g.4584690G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.725C>G MANE Select	ENSP00000293778.7:p.Pro242Arg
ENST00000574412.6:c.725C>G	ENSP00000459592.2:p.Pro242Arg
ENST00000293778.10:c.782C>G	ENSP00000293778.6:p.Pro261Arg
ENST00000574412.5:c.782C>G	ENSP00000459592.1:p.Pro261Arg
ENST00000575168.1:n.556C>G
ENST00000576153.5:n.516C>G
NM_001100812.1:c.782C>G	NP_001094282.1:p.Pro261Arg
NM_022059.3:c.782C>G	NP_071342.2:p.Pro261Arg
NM_022059.4:c.782C>G	NP_071342.2:p.Pro261Arg
NM_001100812.2:c.725C>G	NP_001094282.2:p.Pro242Arg
NM_001386809.1:c.725C>G MANE Select	NP_001373738.1:p.Pro242Arg