Canonical Allele Identifier: CA2244534198

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734639A= , CM000679.2:g.4734639A=	GRCh38
NC_000017.10:g.4637934A= , CM000679.1:g.4637934A=	GRCh37
NC_000017.9:g.4584683A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.732T= MANE Select	ENSP00000293778.7:p.His244=
ENST00000574412.6:c.732T=	ENSP00000459592.2:p.His244=
ENST00000293778.10:c.789T=	ENSP00000293778.6:p.His263=
ENST00000574412.5:c.789T=	ENSP00000459592.1:p.His263=
ENST00000575168.1:n.563T=
ENST00000576153.5:n.523T=
NM_001100812.1:c.789T=	NP_001094282.1:p.His263=
NM_022059.3:c.789T=	NP_071342.2:p.His263=
NM_022059.4:c.789T=	NP_071342.2:p.His263=
NM_001100812.2:c.732T=	NP_001094282.2:p.His244=
NM_001386809.1:c.732T= MANE Select	NP_001373738.1:p.His244=