Canonical Allele Identifier: CA2989583810

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373356_46373357dup , CM000665.2:g.46373356_46373357dup GRCh38
NC_000003.11:g.46414847_46414848dup , CM000665.1:g.46414847_46414848dup GRCh37
NC_000003.10:g.46389851_46389852dup NCBI36
NG_012637.1:g.8215_8216dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.454_455dup (CCR5) MANE Select ENSP00000292303.4:p.Trp153LeufsTer?
ENST00000292303.4:c.454_455dup (CCR5) ENSP00000292303.4:p.Trp153LeufsTer?
ENST00000445772.1:c.454_455dup (CCR5) ENSP00000404881.1:p.Trp153LeufsTer?
NM_000579.3:c.454_455dup (CCR5) NP_000570.1:p.Trp153LeufsTer?
NM_001100168.1:c.454_455dup (CCR5) NP_001093638.1:p.Trp153LeufsTer?
NR_125406.1:n.392-1939_392-1938dup (CCR5AS)
NM_000579.4:c.454_455dup (CCR5) NP_000570.1:p.Trp153LeufsTer?
NM_001100168.2:c.454_455dup (CCR5) NP_001093638.1:p.Trp153LeufsTer?
NM_001394783.1:c.454_455dup (CCR5) MANE Select NP_001381712.1:p.Trp153LeufsTer?