Canonical Allele Identifier: CA2224601311
Gene: CCL17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413472_57413478delinsGAGAAGA , CM000678.2:g.57413472_57413478delinsGAGAAGA GRCh38
NC_000016.9:g.57447384_57447390delinsGAGAAGA , CM000678.1:g.57447384_57447390delinsGAGAAGA GRCh37
NC_000016.8:g.56004885_56004891delinsGAGAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-402_-59-396delinsGAGAAGA MANE Select ENSP00000219244.4:n.-59-402_-59-396delinsGAGAAGA
ENST00000219244.8:c.-59-402_-59-396delinsGAGAAGA ENSP00000219244.4:n.-59-402_-59-396delinsGAGAAGA
NM_002987.2:c.-59-402_-59-396delinsGAGAAGA NP_002978.1:n.-59-402_-59-396delinsGAGAAGA
XM_011523256.1:c.26-402_26-396delinsGAGAAGA XP_011521558.1:n.26-402_26-396delinsGAGAAGA
XM_011523256.2:c.26-402_26-396delinsGAGAAGA XP_011521558.1:n.26-402_26-396delinsGAGAAGA
XM_017023530.1:c.26-399_26-393delinsGAGAAGA XP_016879019.1:n.26-399_26-393delinsGAGAAGA
NM_002987.3:c.-59-402_-59-396delinsGAGAAGA MANE Select NP_002978.1:n.-59-402_-59-396delinsGAGAAGA