Canonical Allele Identifier: CA397281468

Gene: CXCL16

Linked Data

• MyVariant Identifiers: chr17:g.4637923A>C (hg19) ; chr17:g.4734628A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734628A>C , CM000679.2:g.4734628A>C	GRCh38
NC_000017.10:g.4637923A>C , CM000679.1:g.4637923A>C	GRCh37
NC_000017.9:g.4584672A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.743T>G MANE Select	ENSP00000293778.7:p.Val248Gly
ENST00000574412.6:c.743T>G	ENSP00000459592.2:p.Val248Gly
ENST00000293778.10:c.800T>G	ENSP00000293778.6:p.Val267Gly
ENST00000574412.5:c.800T>G	ENSP00000459592.1:p.Val267Gly
ENST00000575168.1:n.574T>G
ENST00000576153.5:n.534T>G
NM_001100812.1:c.800T>G	NP_001094282.1:p.Val267Gly
NM_022059.3:c.800T>G	NP_071342.2:p.Val267Gly
NM_022059.4:c.800T>G	NP_071342.2:p.Val267Gly
NM_001100812.2:c.743T>G	NP_001094282.2:p.Val248Gly
NM_001386809.1:c.743T>G MANE Select	NP_001373738.1:p.Val248Gly