Canonical Allele Identifier: CA2224601378

Gene: CCL17

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57413620C= , CM000678.2:g.57413620C=	GRCh38
NC_000016.9:g.57447532C= , CM000678.1:g.57447532C=	GRCh37
NC_000016.8:g.56005033C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219244.9:c.-59-254C= MANE Select	ENSP00000219244.4:n.-59-254C=
ENST00000219244.8:c.-59-254C=	ENSP00000219244.4:n.-59-254C=
NM_002987.2:c.-59-254C=	NP_002978.1:n.-59-254C=
XM_011523256.1:c.26-254C=	XP_011521558.1:n.26-254C=
XM_011523256.2:c.26-254C=	XP_011521558.1:n.26-254C=
XM_017023530.1:c.26-251C=	XP_016879019.1:n.26-251C=
NM_002987.3:c.-59-254C= MANE Select	NP_002978.1:n.-59-254C=