Canonical Allele Identifier: CA2257712478
Gene: CCL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880231T= , CM000679.2:g.35880231T= GRCh38
NC_000017.9:g.31231348T= NCBI36
NG_015990.1:g.5143A=

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.75A= ENSP00000474412.1:p.Pro25=
ENST00000605140.6:c.75A= MANE Select ENSP00000475057.1:p.Pro25=
ENST00000605509.2:c.75A= ENSP00000474141.2:p.Pro25=
ENST00000651122.1:c.75A= ENSP00000499138.1:p.Pro25=
ENST00000603197.5:c.75A= ENSP00000474412.1:p.Pro25=
ENST00000605140.5:c.75A= ENSP00000475057.1:p.Pro25=
ENST00000605509.1:c.61A=
NM_001278736.1:c.75A= NP_001265665.1:p.Pro25=
NM_002985.2:c.75A= NP_002976.2:p.Pro25=
XR_934696.1:n.197-4151T=
XR_934697.1:n.200-4151T=
XR_001752852.1:n.426+157T=
XR_934696.2:n.91-4151T=
XR_934697.2:n.91-4151T=
NM_001278736.2:c.75A= NP_001265665.1:p.Pro25=
NM_002985.3:c.75A= MANE Select NP_002976.2:p.Pro25=