Canonical Allele Identifier: CA2740411083

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373455_46373456insTTAAAGATA , CM000665.2:g.46373455_46373456insTTAAAGATA GRCh38
NC_000003.11:g.46414946_46414947insTTAAAGATA , CM000665.1:g.46414946_46414947insTTAAAGATA GRCh37
NC_000003.10:g.46389950_46389951insTTAAAGATA NCBI36
NG_012637.1:g.8314_8315insTTAAAGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.553_554insTTAAAGATA (CCR5) MANE Select ENSP00000292303.4:p.Tyr184_Ser185insIleLysAsp
ENST00000292303.4:c.553_554insTTAAAGATA (CCR5) ENSP00000292303.4:p.Tyr184_Ser185insIleLysAsp
ENST00000445772.1:c.553_554insTTAAAGATA (CCR5) ENSP00000404881.1:p.Tyr184_Ser185insIleLysAsp
NM_000579.3:c.553_554insTTAAAGATA (CCR5) NP_000570.1:p.Tyr184_Ser185insIleLysAsp
NM_001100168.1:c.553_554insTTAAAGATA (CCR5) NP_001093638.1:p.Tyr184_Ser185insIleLysAsp
NR_125406.1:n.392-2038_392-2037insATCTTTAAT (CCR5AS)
NM_000579.4:c.553_554insTTAAAGATA (CCR5) NP_000570.1:p.Tyr184_Ser185insIleLysAsp
NM_001100168.2:c.553_554insTTAAAGATA (CCR5) NP_001093638.1:p.Tyr184_Ser185insIleLysAsp
NM_001394783.1:c.553_554insTTAAAGATA (CCR5) MANE Select NP_001381712.1:p.Tyr184_Ser185insIleLysAsp