Canonical Allele Identifier: CA2354587

Gene: CCR5 CCR5AS

Linked Data

• dbSNP Id: rs769057798
• ExAC: 3:46414604 AACCTGGC / A
• gnomAD v2: 3-46414604-AACCTGGC-A
• gnomAD v4: 3-46373113-AACCTGGC-A
• MyVariant Identifiers: chr3:g.46414605_46414611del (hg19) ; chr3:g.46373114_46373120del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46373114_46373120del , CM000665.2:g.46373114_46373120del	GRCh38
NC_000003.11:g.46414605_46414611del , CM000665.1:g.46414605_46414611del	GRCh37
NC_000003.10:g.46389609_46389615del	NCBI36
NG_012637.1:g.7973_7979del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292303.5:c.212_218del (CCR5) MANE Select	ENSP00000292303.4:p.Asn71ThrfsTer?
ENST00000292303.4:c.212_218del (CCR5)	ENSP00000292303.4:p.Asn71ThrfsTer?
ENST00000445772.1:c.212_218del (CCR5)	ENSP00000404881.1:p.Asn71ThrfsTer?
NM_000579.3:c.212_218del (CCR5)	NP_000570.1:p.Asn71ThrfsTer?
NM_001100168.1:c.212_218del (CCR5)	NP_001093638.1:p.Asn71ThrfsTer?
NR_125406.1:n.392-1703_392-1697del (CCR5AS)
NM_000579.4:c.212_218del (CCR5)	NP_000570.1:p.Asn71ThrfsTer?
NM_001100168.2:c.212_218del (CCR5)	NP_001093638.1:p.Asn71ThrfsTer?
NM_001394783.1:c.212_218del (CCR5) MANE Select	NP_001381712.1:p.Asn71ThrfsTer?