Canonical Allele Identifier: CA2665436255

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373191_46373192insTCTTGCTATGGGGA , CM000665.2:g.46373191_46373192insTCTTGCTATGGGGA GRCh38
NC_000003.11:g.46414682_46414683insTCTTGCTATGGGGA , CM000665.1:g.46414682_46414683insTCTTGCTATGGGGA GRCh37
NC_000003.10:g.46389686_46389687insTCTTGCTATGGGGA NCBI36
NG_012637.1:g.8050_8051insTCTTGCTATGGGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.289_290insTCTTGCTATGGGGA (CCR5) MANE Select ENSP00000292303.4:p.Gly97ValfsTer13
ENST00000292303.4:c.289_290insTCTTGCTATGGGGA (CCR5) ENSP00000292303.4:p.Gly97ValfsTer13
ENST00000445772.1:c.289_290insTCTTGCTATGGGGA (CCR5) ENSP00000404881.1:p.Gly97ValfsTer13
NM_000579.3:c.289_290insTCTTGCTATGGGGA (CCR5) NP_000570.1:p.Gly97ValfsTer13
NM_001100168.1:c.289_290insTCTTGCTATGGGGA (CCR5) NP_001093638.1:p.Gly97ValfsTer13
NR_125406.1:n.392-1775_392-1774insTCCCCATAGCAAGA (CCR5AS)
NM_000579.4:c.289_290insTCTTGCTATGGGGA (CCR5) NP_000570.1:p.Gly97ValfsTer13
NM_001100168.2:c.289_290insTCTTGCTATGGGGA (CCR5) NP_001093638.1:p.Gly97ValfsTer13
NM_001394783.1:c.289_290insTCTTGCTATGGGGA (CCR5) MANE Select NP_001381712.1:p.Gly97ValfsTer13