Canonical Allele Identifier: CA2244534100

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734565G= , CM000679.2:g.4734565G=	GRCh38
NC_000017.10:g.4637860G= , CM000679.1:g.4637860G=	GRCh37
NC_000017.9:g.4584609G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+18C= MANE Select	ENSP00000293778.7:n.*23+18C=
ENST00000574412.6:c.*41C=	ENSP00000459592.2:n.*41C=
ENST00000293778.10:c.*23+18C=	ENSP00000293778.6:n.*23+18C=
ENST00000574412.5:c.*41C=	ENSP00000459592.1:n.*41C=
ENST00000576153.5:n.579+18C=
NM_001100812.1:c.*41C=	NP_001094282.1:n.*41C=
NM_022059.3:c.*23+18C=	NP_071342.2:n.*23+18C=
NM_022059.4:c.*23+18C=	NP_071342.2:n.*23+18C=
NM_001100812.2:c.*41C=	NP_001094282.2:n.*41C=
NM_001386809.1:c.*23+18C= MANE Select	NP_001373738.1:n.*23+18C=