Canonical Allele Identifier: CA352469398

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373087A>T , CM000665.2:g.46373087A>T GRCh38
NC_000003.11:g.46414578A>T , CM000665.1:g.46414578A>T GRCh37
NC_000003.10:g.46389582A>T NCBI36
NG_012637.1:g.7946A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.185A>T (CCR5) MANE Select ENSP00000292303.4:p.Lys62Met
ENST00000292303.4:c.185A>T (CCR5) ENSP00000292303.4:p.Lys62Met
ENST00000445772.1:c.185A>T (CCR5) ENSP00000404881.1:p.Lys62Met
NM_000579.3:c.185A>T (CCR5) NP_000570.1:p.Lys62Met
NM_001100168.1:c.185A>T (CCR5) NP_001093638.1:p.Lys62Met
NR_125406.1:n.392-1670T>A (CCR5AS)
NM_000579.4:c.185A>T (CCR5) NP_000570.1:p.Lys62Met
NM_001100168.2:c.185A>T (CCR5) NP_001093638.1:p.Lys62Met
NM_001394783.1:c.185A>T (CCR5) MANE Select NP_001381712.1:p.Lys62Met