Canonical Allele Identifier: CA290054452

Gene: CCL5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35879999A>G , CM000679.2:g.35879999A>G	GRCh38
NC_000017.9:g.31231116A>G	NCBI36
NG_015990.1:g.5375T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603197.6:c.76+231T>C	ENSP00000474412.1:n.76+231T>C
ENST00000605140.6:c.76+231T>C MANE Select	ENSP00000475057.1:n.76+231T>C
ENST00000605509.2:c.76+231T>C	ENSP00000474141.2:n.76+231T>C
ENST00000651122.1:c.76+231T>C	ENSP00000499138.1:n.76+231T>C
ENST00000603197.5:c.76+231T>C	ENSP00000474412.1:n.76+231T>C
ENST00000605140.5:c.76+231T>C	ENSP00000475057.1:n.76+231T>C
ENST00000605509.1:c.62+231T>C
NM_001278736.1:c.76+231T>C	NP_001265665.1:n.76+231T>C
NM_002985.2:c.76+231T>C	NP_002976.2:n.76+231T>C
XR_934696.1:n.197-4383A>G
XR_934697.1:n.200-4383A>G
XR_001752852.1:n.351A>G
XR_934696.2:n.91-4383A>G
XR_934697.2:n.91-4383A>G
NM_001278736.2:c.76+231T>C	NP_001265665.1:n.76+231T>C
NM_002985.3:c.76+231T>C MANE Select	NP_002976.2:n.76+231T>C