Canonical Allele Identifier: CA497526068

Gene: CXCL16

Linked Data

• MyVariant Identifiers: chr17:g.4637919T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734624T>G , CM000679.2:g.4734624T>G	GRCh38
NC_000017.10:g.4637919T>G , CM000679.1:g.4637919T>G	GRCh37
NC_000017.9:g.4584668T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.747A>C MANE Select	ENSP00000293778.7:p.Ala249=
ENST00000574412.6:c.747A>C	ENSP00000459592.2:p.Ala249=
ENST00000293778.10:c.804A>C	ENSP00000293778.6:p.Ala268=
ENST00000574412.5:c.804A>C	ENSP00000459592.1:p.Ala268=
ENST00000575168.1:n.578A>C
ENST00000576153.5:n.538A>C
NM_001100812.1:c.804A>C	NP_001094282.1:p.Ala268=
NM_022059.3:c.804A>C	NP_071342.2:p.Ala268=
NM_022059.4:c.804A>C	NP_071342.2:p.Ala268=
NM_001100812.2:c.747A>C	NP_001094282.2:p.Ala249=
NM_001386809.1:c.747A>C MANE Select	NP_001373738.1:p.Ala249=