Canonical Allele Identifier: CA2244533328

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734082A= , CM000679.2:g.4734082A=	GRCh38
NC_000017.10:g.4637377A= , CM000679.1:g.4637377A=	GRCh37
NC_000017.9:g.4584126A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*421T= MANE Select	ENSP00000293778.7:n.*421T=
ENST00000293778.10:c.*421T=	ENSP00000293778.6:n.*421T=
ENST00000576153.5:n.977T=
NM_022059.3:c.*421T=	NP_071342.2:n.*421T=
NM_022059.4:c.*421T=	NP_071342.2:n.*421T=
NM_001386809.1:c.*421T= MANE Select	NP_001373738.1:n.*421T=