Canonical Allele Identifier: CA2224601328

Gene: CCL17

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57413505_57413506delinsCT , CM000678.2:g.57413505_57413506delinsCT	GRCh38
NC_000016.9:g.57447417_57447418delinsCT , CM000678.1:g.57447417_57447418delinsCT	GRCh37
NC_000016.8:g.56004918_56004919delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219244.9:c.-59-369_-59-368delinsCT MANE Select	ENSP00000219244.4:n.-59-369_-59-368delinsCT
ENST00000219244.8:c.-59-369_-59-368delinsCT	ENSP00000219244.4:n.-59-369_-59-368delinsCT
NM_002987.2:c.-59-369_-59-368delinsCT	NP_002978.1:n.-59-369_-59-368delinsCT
XM_011523256.1:c.26-369_26-368delinsCT	XP_011521558.1:n.26-369_26-368delinsCT
XM_011523256.2:c.26-369_26-368delinsCT	XP_011521558.1:n.26-369_26-368delinsCT
XM_017023530.1:c.26-366_26-365delinsCT	XP_016879019.1:n.26-366_26-365delinsCT
NM_002987.3:c.-59-369_-59-368delinsCT MANE Select	NP_002978.1:n.-59-369_-59-368delinsCT