Canonical Allele Identifier: CA497526150

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734645-C-A
• MyVariant Identifiers: chr17:g.4637940C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734645C>A , CM000679.2:g.4734645C>A	GRCh38
NC_000017.10:g.4637940C>A , CM000679.1:g.4637940C>A	GRCh37
NC_000017.9:g.4584689C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.726G>T MANE Select	ENSP00000293778.7:p.Pro242=
ENST00000574412.6:c.726G>T	ENSP00000459592.2:p.Pro242=
ENST00000293778.10:c.783G>T	ENSP00000293778.6:p.Pro261=
ENST00000574412.5:c.783G>T	ENSP00000459592.1:p.Pro261=
ENST00000575168.1:n.557G>T
ENST00000576153.5:n.517G>T
NM_001100812.1:c.783G>T	NP_001094282.1:p.Pro261=
NM_022059.3:c.783G>T	NP_071342.2:p.Pro261=
NM_022059.4:c.783G>T	NP_071342.2:p.Pro261=
NM_001100812.2:c.726G>T	NP_001094282.2:p.Pro242=
NM_001386809.1:c.726G>T MANE Select	NP_001373738.1:p.Pro242=