Canonical Allele Identifier: CA2244516675

Gene: CXCL16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4738927G= , CM000679.2:g.4738927G=	GRCh38
NC_000017.10:g.4642222G= , CM000679.1:g.4642222G=	GRCh37
NC_000017.9:g.4588971G=	NCBI36
NG_034160.1:g.3913G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001386809.1:c.80-7C= MANE Select	NP_001373738.1:n.80-7C=
ENST00000293778.12:c.80-7C= MANE Select	ENSP00000293778.7:n.80-7C=
NM_001100812.1:c.137-7C=	NP_001094282.1:n.137-7C=
NM_001100812.2:c.80-7C=	NP_001094282.2:n.80-7C=
NM_022059.3:c.137-7C=	NP_071342.2:n.137-7C=
NM_022059.4:c.137-7C=	NP_071342.2:n.137-7C=
ENST00000293778.10:c.137-7C=	ENSP00000293778.6:n.137-7C=
ENST00000573123.1:c.-90C=	ENSP00000460145.1:n.-90C=
ENST00000574412.5:c.137-7C=	ENSP00000459592.1:n.137-7C=
ENST00000574412.6:c.80-7C=	ENSP00000459592.2:n.80-7C=