Canonical Allele Identifier: CA2244535052

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4735268G= , CM000679.2:g.4735268G=	GRCh38
NC_000017.10:g.4638563G= , CM000679.1:g.4638563G=	GRCh37
NC_000017.9:g.4585312G=	NCBI36
NG_034160.1:g.254G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001386809.1:c.542C= MANE Select	NP_001373738.1:p.Ala181=
ENST00000293778.12:c.542C= MANE Select	ENSP00000293778.7:p.Ala181=
NM_001100812.1:c.599C=	NP_001094282.1:p.Ala200=
NM_001100812.2:c.542C=	NP_001094282.2:p.Ala181=
NM_022059.3:c.599C=	NP_071342.2:p.Ala200=
NM_022059.4:c.599C=	NP_071342.2:p.Ala200=
ENST00000293778.10:c.599C=	ENSP00000293778.6:p.Ala200=
ENST00000574412.5:c.599C=	ENSP00000459592.1:p.Ala200=
ENST00000574412.6:c.542C=	ENSP00000459592.2:p.Ala181=
ENST00000575168.1:n.373C=
ENST00000576153.5:n.333C=