Canonical Allele Identifier: CA352472985

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373750A>T , CM000665.2:g.46373750A>T GRCh38
NC_000003.11:g.46415241A>T , CM000665.1:g.46415241A>T GRCh37
NC_000003.10:g.46390245A>T NCBI36
NG_012637.1:g.8609A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.848A>T (CCR5) MANE Select ENSP00000292303.4:p.Glu283Val
ENST00000292303.4:c.848A>T (CCR5) ENSP00000292303.4:p.Glu283Val
ENST00000445772.1:c.848A>T (CCR5) ENSP00000404881.1:p.Glu283Val
NM_000579.3:c.848A>T (CCR5) NP_000570.1:p.Glu283Val
NM_001100168.1:c.848A>T (CCR5) NP_001093638.1:p.Glu283Val
NR_125406.1:n.392-2333T>A (CCR5AS)
NM_000579.4:c.848A>T (CCR5) NP_000570.1:p.Glu283Val
NM_001100168.2:c.848A>T (CCR5) NP_001093638.1:p.Glu283Val
NM_001394783.1:c.848A>T (CCR5) MANE Select NP_001381712.1:p.Glu283Val