Canonical Allele Identifier: CA399220290

Gene: CCL5

Linked Data

• MyVariant Identifiers: chr17:g.35880242A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880242A>T , CM000679.2:g.35880242A>T	GRCh38
NC_000017.9:g.31231359A>T	NCBI36
NG_015990.1:g.5132T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000603197.6:c.64T>A	ENSP00000474412.1:p.Ser22Thr
ENST00000605140.6:c.64T>A MANE Select	ENSP00000475057.1:p.Ser22Thr
ENST00000605509.2:c.64T>A	ENSP00000474141.2:p.Ser22Thr
ENST00000651122.1:c.64T>A	ENSP00000499138.1:p.Ser22Thr
ENST00000603197.5:c.64T>A	ENSP00000474412.1:p.Ser22Thr
ENST00000605140.5:c.64T>A	ENSP00000475057.1:p.Ser22Thr
ENST00000605509.1:c.50T>A
NM_001278736.1:c.64T>A	NP_001265665.1:p.Ser22Thr
NM_002985.2:c.64T>A	NP_002976.2:p.Ser22Thr
XR_934696.1:n.197-4140A>T
XR_934697.1:n.200-4140A>T
XR_001752852.1:n.426+168A>T
XR_934696.2:n.91-4140A>T
XR_934697.2:n.91-4140A>T
NM_001278736.2:c.64T>A	NP_001265665.1:p.Ser22Thr
NM_002985.3:c.64T>A MANE Select	NP_002976.2:p.Ser22Thr