Canonical Allele Identifier: CA2577573858

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373417_46373419del , CM000665.2:g.46373417_46373419del GRCh38
NC_000003.11:g.46414908_46414910del , CM000665.1:g.46414908_46414910del GRCh37
NC_000003.10:g.46389912_46389914del NCBI36
NG_012637.1:g.8276_8278del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.515_517del (CCR5) MANE Select ENSP00000292303.4:p.Glu172del
ENST00000292303.4:c.515_517del (CCR5) ENSP00000292303.4:p.Glu172del
ENST00000445772.1:c.515_517del (CCR5) ENSP00000404881.1:p.Glu172del
NM_000579.3:c.515_517del (CCR5) NP_000570.1:p.Glu172del
NM_001100168.1:c.515_517del (CCR5) NP_001093638.1:p.Glu172del
NR_125406.1:n.392-1999_392-1997del (CCR5AS)
NM_000579.4:c.515_517del (CCR5) NP_000570.1:p.Glu172del
NM_001100168.2:c.515_517del (CCR5) NP_001093638.1:p.Glu172del
NM_001394783.1:c.515_517del (CCR5) MANE Select NP_001381712.1:p.Glu172del