Canonical Allele Identifier: CA497526077

Gene: CXCL16

Linked Data

• MyVariant Identifiers: chr17:g.4637922C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734627C>A , CM000679.2:g.4734627C>A	GRCh38
NC_000017.10:g.4637922C>A , CM000679.1:g.4637922C>A	GRCh37
NC_000017.9:g.4584671C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.744G>T MANE Select	ENSP00000293778.7:p.Val248=
ENST00000574412.6:c.744G>T	ENSP00000459592.2:p.Val248=
ENST00000293778.10:c.801G>T	ENSP00000293778.6:p.Val267=
ENST00000574412.5:c.801G>T	ENSP00000459592.1:p.Val267=
ENST00000575168.1:n.575G>T
ENST00000576153.5:n.535G>T
NM_001100812.1:c.801G>T	NP_001094282.1:p.Val267=
NM_022059.3:c.801G>T	NP_071342.2:p.Val267=
NM_022059.4:c.801G>T	NP_071342.2:p.Val267=
NM_001100812.2:c.744G>T	NP_001094282.2:p.Val248=
NM_001386809.1:c.744G>T MANE Select	NP_001373738.1:p.Val248=