Canonical Allele Identifier: CA8509413
Gene: CCL14 HGNC NCBI
CCL15-CCL14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35984449C>T , CM000679.2:g.35984449C>T GRCh38
NC_000017.10:g.34311485C>T , CM000679.1:g.34311485C>T GRCh37
NC_000017.9:g.31335598C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_032963.4:c.83G>A (CCL14) MANE Select NP_116739.1:p.Gly28Glu
ENST00000618404.5:c.83G>A (CCL14) MANE Select ENSP00000481023.1:p.Gly28Glu
NM_032962.4:c.131G>A (CCL14) NP_116738.1:p.Gly44Glu
NM_032962.5:c.131G>A (CCL14) NP_116738.1:p.Gly44Glu
NM_032963.3:c.83G>A (CCL14) NP_116739.1:p.Gly28Glu
NR_027921.3:n.1120G>A (CCL15-CCL14)
NR_027922.3:n.1072G>A (CCL15-CCL14)
ENST00000610751.4:c.*232G>A (CCL15-CCL14) ENSP00000481940.1:n.*232G>A
ENST00000614009.1:c.149G>A (CCL14) ENSP00000483186.1:p.Gly50Glu
ENST00000616694.1:c.*184G>A (CCL15-CCL14) ENSP00000481402.1:n.*184G>A
ENST00000618404.4:c.83G>A (CCL14) ENSP00000481023.1:p.Gly28Glu
ENST00000620991.1:c.83G>A (CCL14) ENSP00000484818.1:p.Gly28Glu
ENST00000622526.1:c.131G>A (CCL14) ENSP00000479097.1:p.Gly44Glu