Canonical Allele Identifier: CA2665436258

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373195_46373196insAGACA , CM000665.2:g.46373195_46373196insAGACA GRCh38
NC_000003.11:g.46414686_46414687insAGACA , CM000665.1:g.46414686_46414687insAGACA GRCh37
NC_000003.10:g.46389690_46389691insAGACA NCBI36
NG_012637.1:g.8054_8055insAGACA

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.293_294insAGACA (CCR5) MANE Select ENSP00000292303.4:p.Asn98LysfsTer9
ENST00000292303.4:c.293_294insAGACA (CCR5) ENSP00000292303.4:p.Asn98LysfsTer9
ENST00000445772.1:c.293_294insAGACA (CCR5) ENSP00000404881.1:p.Asn98LysfsTer9
NM_000579.3:c.293_294insAGACA (CCR5) NP_000570.1:p.Asn98LysfsTer9
NM_001100168.1:c.293_294insAGACA (CCR5) NP_001093638.1:p.Asn98LysfsTer9
NR_125406.1:n.392-1778_392-1777insGTCTT (CCR5AS)
NM_000579.4:c.293_294insAGACA (CCR5) NP_000570.1:p.Asn98LysfsTer9
NM_001100168.2:c.293_294insAGACA (CCR5) NP_001093638.1:p.Asn98LysfsTer9
NM_001394783.1:c.293_294insAGACA (CCR5) MANE Select NP_001381712.1:p.Asn98LysfsTer9