Canonical Allele Identifier: CA2733521324

Gene: CCL5

Linked Data

• dbSNP Id: rs2144037857

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880226_35880229dup , CM000679.2:g.35880226_35880229dup	GRCh38
NC_000017.9:g.31231343_31231346dup	NCBI36
NG_015990.1:g.5147_5150dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603197.6:c.76+3_76+6dup	ENSP00000474412.1:n.76+3_76+6dup
ENST00000605140.6:c.76+3_76+6dup MANE Select	ENSP00000475057.1:n.76+3_76+6dup
ENST00000605509.2:c.76+3_76+6dup	ENSP00000474141.2:n.76+3_76+6dup
ENST00000651122.1:c.76+3_76+6dup	ENSP00000499138.1:n.76+3_76+6dup
ENST00000603197.5:c.76+3_76+6dup	ENSP00000474412.1:n.76+3_76+6dup
ENST00000605140.5:c.76+3_76+6dup	ENSP00000475057.1:n.76+3_76+6dup
ENST00000605509.1:c.62+3_62+6dup
NM_001278736.1:c.76+3_76+6dup	NP_001265665.1:n.76+3_76+6dup
NM_002985.2:c.76+3_76+6dup	NP_002976.2:n.76+3_76+6dup
XR_934696.1:n.197-4156_197-4153dup
XR_934697.1:n.200-4156_200-4153dup
XR_001752852.1:n.426+152_426+155dup
XR_934696.2:n.91-4156_91-4153dup
XR_934697.2:n.91-4156_91-4153dup
NM_001278736.2:c.76+3_76+6dup	NP_001265665.1:n.76+3_76+6dup
NM_002985.3:c.76+3_76+6dup MANE Select	NP_002976.2:n.76+3_76+6dup