Canonical Allele Identifier: CA290051494

Gene: CCL5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35872637A>T , CM000679.2:g.35872637A>T	GRCh38
NC_000017.9:g.31223754A>T	NCBI36
NG_015990.1:g.12737T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603197.6:c.189-173T>A	ENSP00000474412.1:n.189-173T>A
ENST00000605140.6:c.189-173T>A MANE Select	ENSP00000475057.1:n.189-173T>A
ENST00000605509.2:c.189-173T>A	ENSP00000474141.2:n.189-173T>A
ENST00000651122.1:c.271-173T>A	ENSP00000499138.1:n.271-173T>A
ENST00000603197.5:c.189-173T>A	ENSP00000474412.1:n.189-173T>A
ENST00000605140.5:c.189-173T>A	ENSP00000475057.1:n.189-173T>A
ENST00000605509.1:c.257-173T>A
NM_001278736.1:c.271-173T>A	NP_001265665.1:n.271-173T>A
NM_002985.2:c.189-173T>A	NP_002976.2:n.189-173T>A
XR_934696.1:n.196+3519A>T
XR_934697.1:n.199+3519A>T
XR_934696.2:n.90+3519A>T
XR_934697.2:n.90+3519A>T
NM_001278736.2:c.271-173T>A	NP_001265665.1:n.271-173T>A
NM_002985.3:c.189-173T>A MANE Select	NP_002976.2:n.189-173T>A