Canonical Allele Identifier: CA983289897

Gene: CCL5

Linked Data

• dbSNP Id: rs749466056
• gnomAD v3: 17-35880214-C-A
• gnomAD v4: 17-35880214-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880214C>A , CM000679.2:g.35880214C>A	GRCh38
NC_000017.9:g.31231331C>A	NCBI36
NG_015990.1:g.5160G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000603197.6:c.76+16G>T	ENSP00000474412.1:n.76+16G>T
ENST00000605140.6:c.76+16G>T MANE Select	ENSP00000475057.1:n.76+16G>T
ENST00000605509.2:c.76+16G>T	ENSP00000474141.2:n.76+16G>T
ENST00000651122.1:c.76+16G>T	ENSP00000499138.1:n.76+16G>T
ENST00000603197.5:c.76+16G>T	ENSP00000474412.1:n.76+16G>T
ENST00000605140.5:c.76+16G>T	ENSP00000475057.1:n.76+16G>T
ENST00000605509.1:c.62+16G>T
NM_001278736.1:c.76+16G>T	NP_001265665.1:n.76+16G>T
NM_002985.2:c.76+16G>T	NP_002976.2:n.76+16G>T
XR_934696.1:n.197-4168C>A
XR_934697.1:n.200-4168C>A
XR_001752852.1:n.426+140C>A
XR_934696.2:n.91-4168C>A
XR_934697.2:n.91-4168C>A
NM_001278736.2:c.76+16G>T	NP_001265665.1:n.76+16G>T
NM_002985.3:c.76+16G>T MANE Select	NP_002976.2:n.76+16G>T