Canonical Allele Identifier: CA2224601238
Gene: CCL17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413303G= , CM000678.2:g.57413303G= GRCh38
NC_000016.9:g.57447215G= , CM000678.1:g.57447215G= GRCh37
NC_000016.8:g.56004716G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-571G= MANE Select ENSP00000219244.4:n.-59-571G=
ENST00000219244.8:c.-59-571G= ENSP00000219244.4:n.-59-571G=
NM_002987.2:c.-59-571G= NP_002978.1:n.-59-571G=
XM_011523256.1:c.26-571G= XP_011521558.1:n.26-571G=
XM_011523256.2:c.26-571G= XP_011521558.1:n.26-571G=
XM_017023530.1:c.26-568G= XP_016879019.1:n.26-568G=
NM_002987.3:c.-59-571G= MANE Select NP_002978.1:n.-59-571G=
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