Canonical Allele Identifier: CA2354612

Linked Data

dbSNP Id: rs776790089

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373212_46373213del , CM000665.2:g.46373212_46373213del GRCh38
NC_000003.11:g.46414703_46414704del , CM000665.1:g.46414703_46414704del GRCh37
NC_000003.10:g.46389707_46389708del NCBI36
NG_012637.1:g.8071_8072del

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.310_311del (CCR5) MANE Select ENSP00000292303.4:p.Leu104AspfsTer22
ENST00000292303.4:c.310_311del (CCR5) ENSP00000292303.4:p.Leu104AspfsTer22
ENST00000445772.1:c.310_311del (CCR5) ENSP00000404881.1:p.Leu104AspfsTer22
NM_000579.3:c.310_311del (CCR5) NP_000570.1:p.Leu104AspfsTer22
NM_001100168.1:c.310_311del (CCR5) NP_001093638.1:p.Leu104AspfsTer22
NR_125406.1:n.392-1796_392-1795del (CCR5AS)
NM_000579.4:c.310_311del (CCR5) NP_000570.1:p.Leu104AspfsTer22
NM_001100168.2:c.310_311del (CCR5) NP_001093638.1:p.Leu104AspfsTer22
NM_001394783.1:c.310_311del (CCR5) MANE Select NP_001381712.1:p.Leu104AspfsTer22