Canonical Allele Identifier: CA2224601326
Gene: CCL17 HGNC NCBI

Linked Data

dbSNP Id: rs1902818400
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413506_57413513del , CM000678.2:g.57413506_57413513del GRCh38
NC_000016.9:g.57447418_57447425del , CM000678.1:g.57447418_57447425del GRCh37
NC_000016.8:g.56004919_56004926del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-368_-59-361del MANE Select ENSP00000219244.4:n.-59-368_-59-361del
ENST00000219244.8:c.-59-368_-59-361del ENSP00000219244.4:n.-59-368_-59-361del
NM_002987.2:c.-59-368_-59-361del NP_002978.1:n.-59-368_-59-361del
XM_011523256.1:c.26-368_26-361del XP_011521558.1:n.26-368_26-361del
XM_011523256.2:c.26-368_26-361del XP_011521558.1:n.26-368_26-361del
XM_017023530.1:c.26-365_26-358del XP_016879019.1:n.26-365_26-358del
NM_002987.3:c.-59-368_-59-361del MANE Select NP_002978.1:n.-59-368_-59-361del
Search 100 bp 5'
Search 100 bp 3'