Canonical Allele Identifier: CA2257712602
Gene: CCL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880345C= , CM000679.2:g.35880345C= GRCh38
NC_000017.9:g.31231462C= NCBI36
NG_015990.1:g.5029G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000603197.6:c.-40G= ENSP00000474412.1:n.-40G=
ENST00000605140.6:c.-40G= MANE Select ENSP00000475057.1:n.-40G=
ENST00000605509.2:c.-17-23G= ENSP00000474141.2:n.-17-23G=
ENST00000651122.1:c.-40G= ENSP00000499138.1:n.-40G=
ENST00000603197.5:c.-40G= ENSP00000474412.1:n.-40G=
ENST00000605140.5:c.-17-23G= ENSP00000475057.1:n.-17-23G=
NM_001278736.1:c.-40G= NP_001265665.1:n.-40G=
NM_002985.2:c.-40G= NP_002976.2:n.-40G=
XR_934696.1:n.197-4037C=
XR_934697.1:n.200-4037C=
XR_001752852.1:n.426+271C=
XR_934696.2:n.91-4037C=
XR_934697.2:n.91-4037C=
NM_001278736.2:c.-40G= NP_001265665.1:n.-40G=
NM_002985.3:c.-40G= MANE Select NP_002976.2:n.-40G=