Canonical Allele Identifier: CA2224601304
Gene: CCL17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57413463A= , CM000678.2:g.57413463A= GRCh38
NC_000016.9:g.57447375A= , CM000678.1:g.57447375A= GRCh37
NC_000016.8:g.56004876A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219244.9:c.-59-411A= MANE Select ENSP00000219244.4:n.-59-411A=
ENST00000219244.8:c.-59-411A= ENSP00000219244.4:n.-59-411A=
NM_002987.2:c.-59-411A= NP_002978.1:n.-59-411A=
XM_011523256.1:c.26-411A= XP_011521558.1:n.26-411A=
XM_011523256.2:c.26-411A= XP_011521558.1:n.26-411A=
XM_017023530.1:c.26-408A= XP_016879019.1:n.26-408A=
NM_002987.3:c.-59-411A= MANE Select NP_002978.1:n.-59-411A=