Canonical Allele Identifier: CA397281369

Gene: CXCL16

Linked Data

• MyVariant Identifiers: chr17:g.4637901T>C (hg19) ; chr17:g.4734606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734606T>C , CM000679.2:g.4734606T>C	GRCh38
NC_000017.10:g.4637901T>C , CM000679.1:g.4637901T>C	GRCh37
NC_000017.9:g.4584650T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000293778.12:c.765A>G MANE Select	ENSP00000293778.7:p.Ter255Trp
ENST00000574412.6:c.765A>G	ENSP00000459592.2:p.Ter255Trp
ENST00000293778.10:c.822A>G	ENSP00000293778.6:p.Ter274Trp
ENST00000574412.5:c.822A>G	ENSP00000459592.1:p.Ter274Trp
ENST00000575168.1:n.596A>G
ENST00000576153.5:n.556A>G
NM_001100812.1:c.822A>G	NP_001094282.1:p.Ter274Trp
NM_022059.3:c.822A>G	NP_071342.2:p.Ter274Trp
NM_022059.4:c.822A>G	NP_071342.2:p.Ter274Trp
NM_001100812.2:c.765A>G	NP_001094282.2:p.Ter255Trp
NM_001386809.1:c.765A>G MANE Select	NP_001373738.1:p.Ter255Trp