Canonical Allele Identifier: CA907591713
Gene: CCR5 HGNC NCBI
CCR5AS HGNC NCBI

Linked Data

dbSNP Id: rs1444201344
gnomAD v3: 3-46373133-GT-G
gnomAD v4: 3-46373133-GT-G
MyVariant Identifiers: chr3:g.46414625del (hg19) chr3:g.46373134del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373138del , CM000665.2:g.46373138del GRCh38
NC_000003.11:g.46414629del , CM000665.1:g.46414629del GRCh37
NC_000003.10:g.46389633del NCBI36
NG_012637.1:g.7997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.236del (CCR5) MANE Select ENSP00000292303.4:p.Phe79SerfsTer26
ENST00000292303.4:c.236del (CCR5) ENSP00000292303.4:p.Phe79SerfsTer26
ENST00000445772.1:c.236del (CCR5) ENSP00000404881.1:p.Phe79SerfsTer26
NM_000579.3:c.236del (CCR5) NP_000570.1:p.Phe79SerfsTer26
NM_001100168.1:c.236del (CCR5) NP_001093638.1:p.Phe79SerfsTer26
NR_125406.1:n.392-1717del (CCR5AS)
NM_000579.4:c.236del (CCR5) NP_000570.1:p.Phe79SerfsTer26
NM_001100168.2:c.236del (CCR5) NP_001093638.1:p.Phe79SerfsTer26
NM_001394783.1:c.236del (CCR5) MANE Select NP_001381712.1:p.Phe79SerfsTer26
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