Canonical Allele Identifier: CA2637310312
Gene: CCL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880334C>A , CM000679.2:g.35880334C>A GRCh38
NC_000017.9:g.31231451C>A NCBI36
NG_015990.1:g.5040G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.-29G>T ENSP00000474412.1:n.-29G>T
ENST00000605140.6:c.-29G>T MANE Select ENSP00000475057.1:n.-29G>T
ENST00000605509.2:c.-17-12G>T ENSP00000474141.2:n.-17-12G>T
ENST00000651122.1:c.-29G>T ENSP00000499138.1:n.-29G>T
ENST00000603197.5:c.-29G>T ENSP00000474412.1:n.-29G>T
ENST00000605140.5:c.-17-12G>T ENSP00000475057.1:n.-17-12G>T
NM_001278736.1:c.-29G>T NP_001265665.1:n.-29G>T
NM_002985.2:c.-29G>T NP_002976.2:n.-29G>T
XR_934696.1:n.197-4048C>A
XR_934697.1:n.200-4048C>A
XR_001752852.1:n.426+260C>A
XR_934696.2:n.91-4048C>A
XR_934697.2:n.91-4048C>A
NM_001278736.2:c.-29G>T NP_001265665.1:n.-29G>T
NM_002985.3:c.-29G>T MANE Select NP_002976.2:n.-29G>T