Canonical Allele Identifier: CA728422197

Gene: CCL5

Linked Data

• dbSNP Id: rs1380853934
• gnomAD v3: 17-35880231-T-A
• gnomAD v4: 17-35880231-T-A
• MyVariant Identifiers: chr17:g.35880231T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880231T>A , CM000679.2:g.35880231T>A	GRCh38
NC_000017.9:g.31231348T>A	NCBI36
NG_015990.1:g.5143A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603197.6:c.75A>T	ENSP00000474412.1:p.Pro25=
ENST00000605140.6:c.75A>T MANE Select	ENSP00000475057.1:p.Pro25=
ENST00000605509.2:c.75A>T	ENSP00000474141.2:p.Pro25=
ENST00000651122.1:c.75A>T	ENSP00000499138.1:p.Pro25=
ENST00000603197.5:c.75A>T	ENSP00000474412.1:p.Pro25=
ENST00000605140.5:c.75A>T	ENSP00000475057.1:p.Pro25=
ENST00000605509.1:c.61A>T
NM_001278736.1:c.75A>T	NP_001265665.1:p.Pro25=
NM_002985.2:c.75A>T	NP_002976.2:p.Pro25=
XR_934696.1:n.197-4151T>A
XR_934697.1:n.200-4151T>A
XR_001752852.1:n.426+157T>A
XR_934696.2:n.91-4151T>A
XR_934697.2:n.91-4151T>A
NM_001278736.2:c.75A>T	NP_001265665.1:p.Pro25=
NM_002985.3:c.75A>T MANE Select	NP_002976.2:p.Pro25=