Canonical Allele Identifier: CA2224601342
Gene: CCL17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413538C= , CM000678.2:g.57413538C= GRCh38
NC_000016.9:g.57447450C= , CM000678.1:g.57447450C= GRCh37
NC_000016.8:g.56004951C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-336C= MANE Select ENSP00000219244.4:n.-59-336C=
ENST00000219244.8:c.-59-336C= ENSP00000219244.4:n.-59-336C=
NM_002987.2:c.-59-336C= NP_002978.1:n.-59-336C=
XM_011523256.1:c.26-336C= XP_011521558.1:n.26-336C=
XM_011523256.2:c.26-336C= XP_011521558.1:n.26-336C=
XM_017023530.1:c.26-333C= XP_016879019.1:n.26-333C=
NM_002987.3:c.-59-336C= MANE Select NP_002978.1:n.-59-336C=
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