Canonical Allele Identifier: CA2257712565
Gene: CCL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880301T= , CM000679.2:g.35880301T= GRCh38
NC_000017.9:g.31231418T= NCBI36
NG_015990.1:g.5073A=

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.5A= ENSP00000474412.1:p.Lys2=
ENST00000605140.6:c.5A= MANE Select ENSP00000475057.1:p.Lys2=
ENST00000605509.2:c.5A= ENSP00000474141.2:p.Lys2=
ENST00000651122.1:c.5A= ENSP00000499138.1:p.Lys2=
ENST00000603197.5:c.5A= ENSP00000474412.1:p.Lys2=
ENST00000605140.5:c.5A= ENSP00000475057.1:p.Lys2=
NM_001278736.1:c.5A= NP_001265665.1:p.Lys2=
NM_002985.2:c.5A= NP_002976.2:p.Lys2=
XR_934696.1:n.197-4081T=
XR_934697.1:n.200-4081T=
XR_001752852.1:n.426+227T=
XR_934696.2:n.91-4081T=
XR_934697.2:n.91-4081T=
NM_001278736.2:c.5A= NP_001265665.1:p.Lys2=
NM_002985.3:c.5A= MANE Select NP_002976.2:p.Lys2=