Canonical Allele Identifier: CA399220266
Gene: CCL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.35880236A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880236A>G , CM000679.2:g.35880236A>G GRCh38
NC_000017.9:g.31231353A>G NCBI36
NG_015990.1:g.5138T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.70T>C ENSP00000474412.1:p.Ser24Pro
ENST00000605140.6:c.70T>C MANE Select ENSP00000475057.1:p.Ser24Pro
ENST00000605509.2:c.70T>C ENSP00000474141.2:p.Ser24Pro
ENST00000651122.1:c.70T>C ENSP00000499138.1:p.Ser24Pro
ENST00000603197.5:c.70T>C ENSP00000474412.1:p.Ser24Pro
ENST00000605140.5:c.70T>C ENSP00000475057.1:p.Ser24Pro
ENST00000605509.1:c.56T>C
NM_001278736.1:c.70T>C NP_001265665.1:p.Ser24Pro
NM_002985.2:c.70T>C NP_002976.2:p.Ser24Pro
XR_934696.1:n.197-4146A>G
XR_934697.1:n.200-4146A>G
XR_001752852.1:n.426+162A>G
XR_934696.2:n.91-4146A>G
XR_934697.2:n.91-4146A>G
NM_001278736.2:c.70T>C NP_001265665.1:p.Ser24Pro
NM_002985.3:c.70T>C MANE Select NP_002976.2:p.Ser24Pro