Canonical Allele Identifier: CA2244534102

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916094200

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734566_4734567insCTTT , CM000679.2:g.4734566_4734567insCTTT	GRCh38
NC_000017.10:g.4637861_4637862insCTTT , CM000679.1:g.4637861_4637862insCTTT	GRCh37
NC_000017.9:g.4584610_4584611insCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+16_*23+17insAAAG MANE Select	ENSP00000293778.7:n.*23+16_*23+17insAAAG
ENST00000574412.6:c.*39_*40insAAAG	ENSP00000459592.2:n.*39_*40insAAAG
ENST00000293778.10:c.*23+16_*23+17insAAAG	ENSP00000293778.6:n.*23+16_*23+17insAAAG
ENST00000574412.5:c.*39_*40insAAAG	ENSP00000459592.1:n.*39_*40insAAAG
ENST00000576153.5:n.579+16_579+17insAAAG
NM_001100812.1:c.*39_*40insAAAG	NP_001094282.1:n.*39_*40insAAAG
NM_022059.3:c.*23+16_*23+17insAAAG	NP_071342.2:n.*23+16_*23+17insAAAG
NM_022059.4:c.*23+16_*23+17insAAAG	NP_071342.2:n.*23+16_*23+17insAAAG
NM_001100812.2:c.*39_*40insAAAG	NP_001094282.2:n.*39_*40insAAAG
NM_001386809.1:c.*23+16_*23+17insAAAG MANE Select	NP_001373738.1:n.*23+16_*23+17insAAAG