Canonical Allele Identifier: CA1362082582

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373396T= , CM000665.2:g.46373396T= GRCh38
NC_000003.11:g.46414887T= , CM000665.1:g.46414887T= GRCh37
NC_000003.10:g.46389891T= NCBI36
NG_012637.1:g.8255T=

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.494T= (CCR5) MANE Select ENSP00000292303.4:p.Ile165=
ENST00000292303.4:c.494T= (CCR5) ENSP00000292303.4:p.Ile165=
ENST00000445772.1:c.494T= (CCR5) ENSP00000404881.1:p.Ile165=
NM_000579.3:c.494T= (CCR5) NP_000570.1:p.Ile165=
NM_001100168.1:c.494T= (CCR5) NP_001093638.1:p.Ile165=
NR_125406.1:n.392-1979A= (CCR5AS)
NM_000579.4:c.494T= (CCR5) NP_000570.1:p.Ile165=
NM_001100168.2:c.494T= (CCR5) NP_001093638.1:p.Ile165=
NM_001394783.1:c.494T= (CCR5) MANE Select NP_001381712.1:p.Ile165=