Canonical Allele Identifier: CA2244534121

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734590A= , CM000679.2:g.4734590A=	GRCh38
NC_000017.10:g.4637885A= , CM000679.1:g.4637885A=	GRCh37
NC_000017.9:g.4584634A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*16T= MANE Select	ENSP00000293778.7:n.*16T=
ENST00000574412.6:c.*16T=	ENSP00000459592.2:n.*16T=
ENST00000293778.10:c.*16T=	ENSP00000293778.6:n.*16T=
ENST00000574412.5:c.*16T=	ENSP00000459592.1:n.*16T=
ENST00000575168.1:n.612T=
ENST00000576153.5:n.572T=
NM_001100812.1:c.*16T=	NP_001094282.1:n.*16T=
NM_022059.3:c.*16T=	NP_071342.2:n.*16T=
NM_022059.4:c.*16T=	NP_071342.2:n.*16T=
NM_001100812.2:c.*16T=	NP_001094282.2:n.*16T=
NM_001386809.1:c.*16T= MANE Select	NP_001373738.1:n.*16T=