Canonical Allele Identifier: CA2637310295
Gene: CCL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880324T>C , CM000679.2:g.35880324T>C GRCh38
NC_000017.9:g.31231441T>C NCBI36
NG_015990.1:g.5050A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.-19A>G ENSP00000474412.1:n.-19A>G
ENST00000605140.6:c.-19A>G MANE Select ENSP00000475057.1:n.-19A>G
ENST00000605509.2:c.-17-2A>G ENSP00000474141.2:n.-17-2A>G
ENST00000651122.1:c.-19A>G ENSP00000499138.1:n.-19A>G
ENST00000603197.5:c.-19A>G ENSP00000474412.1:n.-19A>G
ENST00000605140.5:c.-17-2A>G ENSP00000475057.1:n.-17-2A>G
NM_001278736.1:c.-19A>G NP_001265665.1:n.-19A>G
NM_002985.2:c.-19A>G NP_002976.2:n.-19A>G
XR_934696.1:n.197-4058T>C
XR_934697.1:n.200-4058T>C
XR_001752852.1:n.426+250T>C
XR_934696.2:n.91-4058T>C
XR_934697.2:n.91-4058T>C
NM_001278736.2:c.-19A>G NP_001265665.1:n.-19A>G
NM_002985.3:c.-19A>G MANE Select NP_002976.2:n.-19A>G