Canonical Allele Identifier: CA2257712601
Gene: CCL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880344T= , CM000679.2:g.35880344T= GRCh38
NC_000017.9:g.31231461T= NCBI36
NG_015990.1:g.5030A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000603197.6:c.-39A= ENSP00000474412.1:n.-39A=
ENST00000605140.6:c.-39A= MANE Select ENSP00000475057.1:n.-39A=
ENST00000605509.2:c.-17-22A= ENSP00000474141.2:n.-17-22A=
ENST00000651122.1:c.-39A= ENSP00000499138.1:n.-39A=
ENST00000603197.5:c.-39A= ENSP00000474412.1:n.-39A=
ENST00000605140.5:c.-17-22A= ENSP00000475057.1:n.-17-22A=
NM_001278736.1:c.-39A= NP_001265665.1:n.-39A=
NM_002985.2:c.-39A= NP_002976.2:n.-39A=
XR_934696.1:n.197-4038T=
XR_934697.1:n.200-4038T=
XR_001752852.1:n.426+270T=
XR_934696.2:n.91-4038T=
XR_934697.2:n.91-4038T=
NM_001278736.2:c.-39A= NP_001265665.1:n.-39A=
NM_002985.3:c.-39A= MANE Select NP_002976.2:n.-39A=