Canonical Allele Identifier: CA2257712476
Gene: CCL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880230A= , CM000679.2:g.35880230A= GRCh38
NC_000017.9:g.31231347A= NCBI36
NG_015990.1:g.5144T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000603197.6:c.76T= ENSP00000474412.1:p.Tyr26=
ENST00000605140.6:c.76T= MANE Select ENSP00000475057.1:p.Tyr26=
ENST00000605509.2:c.76T= ENSP00000474141.2:p.Tyr26=
ENST00000651122.1:c.76T= ENSP00000499138.1:p.Tyr26=
ENST00000603197.5:c.76T= ENSP00000474412.1:p.Tyr26=
ENST00000605140.5:c.76T= ENSP00000475057.1:p.Tyr26=
ENST00000605509.1:c.62T=
NM_001278736.1:c.76T= NP_001265665.1:p.Tyr26=
NM_002985.2:c.76T= NP_002976.2:p.Tyr26=
XR_934696.1:n.197-4152A=
XR_934697.1:n.200-4152A=
XR_001752852.1:n.426+156A=
XR_934696.2:n.91-4152A=
XR_934697.2:n.91-4152A=
NM_001278736.2:c.76T= NP_001265665.1:p.Tyr26=
NM_002985.3:c.76T= MANE Select NP_002976.2:p.Tyr26=