Canonical Allele Identifier: CA722066802
Gene: CCL17 HGNC NCBI

Linked Data

dbSNP Id: rs1333022166

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413473_57413478del , CM000678.2:g.57413473_57413478del GRCh38
NC_000016.9:g.57447385_57447390del , CM000678.1:g.57447385_57447390del GRCh37
NC_000016.8:g.56004886_56004891del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-401_-59-396del MANE Select ENSP00000219244.4:n.-59-401_-59-396del
ENST00000219244.8:c.-59-401_-59-396del ENSP00000219244.4:n.-59-401_-59-396del
NM_002987.2:c.-59-401_-59-396del NP_002978.1:n.-59-401_-59-396del
XM_011523256.1:c.26-401_26-396del XP_011521558.1:n.26-401_26-396del
XM_011523256.2:c.26-401_26-396del XP_011521558.1:n.26-401_26-396del
XM_017023530.1:c.26-398_26-393del XP_016879019.1:n.26-398_26-393del
NM_002987.3:c.-59-401_-59-396del MANE Select NP_002978.1:n.-59-401_-59-396del