Canonical Allele Identifier: CA497526165

Gene: CXCL16

Linked Data

• MyVariant Identifiers: chr17:g.4637943C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734648C>G , CM000679.2:g.4734648C>G	GRCh38
NC_000017.10:g.4637943C>G , CM000679.1:g.4637943C>G	GRCh37
NC_000017.9:g.4584692C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.723G>C MANE Select	ENSP00000293778.7:p.Leu241=
ENST00000574412.6:c.723G>C	ENSP00000459592.2:p.Leu241=
ENST00000293778.10:c.780G>C	ENSP00000293778.6:p.Leu260=
ENST00000574412.5:c.780G>C	ENSP00000459592.1:p.Leu260=
ENST00000575168.1:n.554G>C
ENST00000576153.5:n.514G>C
NM_001100812.1:c.780G>C	NP_001094282.1:p.Leu260=
NM_022059.3:c.780G>C	NP_071342.2:p.Leu260=
NM_022059.4:c.780G>C	NP_071342.2:p.Leu260=
NM_001100812.2:c.723G>C	NP_001094282.2:p.Leu241=
NM_001386809.1:c.723G>C MANE Select	NP_001373738.1:p.Leu241=