Canonical Allele Identifier: CA2244534117

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734582C= , CM000679.2:g.4734582C=	GRCh38
NC_000017.10:g.4637877C= , CM000679.1:g.4637877C=	GRCh37
NC_000017.9:g.4584626C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+1G= MANE Select	ENSP00000293778.7:n.*23+1G=
ENST00000574412.6:c.*24G=	ENSP00000459592.2:n.*24G=
ENST00000293778.10:c.*23+1G=	ENSP00000293778.6:n.*23+1G=
ENST00000574412.5:c.*24G=	ENSP00000459592.1:n.*24G=
ENST00000576153.5:n.579+1G=
NM_001100812.1:c.*24G=	NP_001094282.1:n.*24G=
NM_022059.3:c.*23+1G=	NP_071342.2:n.*23+1G=
NM_022059.4:c.*23+1G=	NP_071342.2:n.*23+1G=
NM_001100812.2:c.*24G=	NP_001094282.2:n.*24G=
NM_001386809.1:c.*23+1G= MANE Select	NP_001373738.1:n.*23+1G=