Canonical Allele Identifier: CA543041134

Gene: CCR5 CCR5AS

Linked Data

• dbSNP Id: rs1215591945
• gnomAD v2: 3-46414791-CTG-C
• gnomAD v4: 3-46373300-CTG-C
• MyVariant Identifiers: chr3:g.46414792_46414793del (hg19) ; chr3:g.46373301_46373302del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46373304_46373305del , CM000665.2:g.46373304_46373305del	GRCh38
NC_000003.11:g.46414795_46414796del , CM000665.1:g.46414795_46414796del	GRCh37
NC_000003.10:g.46389799_46389800del	NCBI36
NG_012637.1:g.8163_8164del

Transcript Alleles

HGVS	Amino-acid change
ENST00000292303.5:c.402_403del (CCR5) MANE Select	ENSP00000292303.4:p.Phe135CysfsTer?
ENST00000292303.4:c.402_403del (CCR5)	ENSP00000292303.4:p.Phe135CysfsTer?
ENST00000445772.1:c.402_403del (CCR5)	ENSP00000404881.1:p.Phe135CysfsTer?
NM_000579.3:c.402_403del (CCR5)	NP_000570.1:p.Phe135CysfsTer?
NM_001100168.1:c.402_403del (CCR5)	NP_001093638.1:p.Phe135CysfsTer?
NR_125406.1:n.392-1885_392-1884del (CCR5AS)
NM_000579.4:c.402_403del (CCR5)	NP_000570.1:p.Phe135CysfsTer?
NM_001100168.2:c.402_403del (CCR5)	NP_001093638.1:p.Phe135CysfsTer?
NM_001394783.1:c.402_403del (CCR5) MANE Select	NP_001381712.1:p.Phe135CysfsTer?