Canonical Allele Identifier: CA2224601363
Gene: CCL17 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413584G= , CM000678.2:g.57413584G= GRCh38
NC_000016.9:g.57447496G= , CM000678.1:g.57447496G= GRCh37
NC_000016.8:g.56004997G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-290G= MANE Select ENSP00000219244.4:n.-59-290G=
ENST00000219244.8:c.-59-290G= ENSP00000219244.4:n.-59-290G=
NM_002987.2:c.-59-290G= NP_002978.1:n.-59-290G=
XM_011523256.1:c.26-290G= XP_011521558.1:n.26-290G=
XM_011523256.2:c.26-290G= XP_011521558.1:n.26-290G=
XM_017023530.1:c.26-287G= XP_016879019.1:n.26-287G=
NM_002987.3:c.-59-290G= MANE Select NP_002978.1:n.-59-290G=
Search 100 bp 5'
Search 100 bp 3'