Canonical Allele Identifier: CA1362082831

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373898C= , CM000665.2:g.46373898C= GRCh38
NC_000003.11:g.46415389C= , CM000665.1:g.46415389C= GRCh37
NC_000003.10:g.46390393C= NCBI36
NG_012637.1:g.8757C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.996C= (CCR5) MANE Select ENSP00000292303.4:p.Pro332=
ENST00000292303.4:c.996C= (CCR5) ENSP00000292303.4:p.Pro332=
ENST00000445772.1:c.996C= (CCR5) ENSP00000404881.1:p.Pro332=
NM_000579.3:c.996C= (CCR5) NP_000570.1:p.Pro332=
NM_001100168.1:c.996C= (CCR5) NP_001093638.1:p.Pro332=
NR_125406.1:n.392-2481G= (CCR5AS)
NM_000579.4:c.996C= (CCR5) NP_000570.1:p.Pro332=
NM_001100168.2:c.996C= (CCR5) NP_001093638.1:p.Pro332=
NM_001394783.1:c.996C= (CCR5) MANE Select NP_001381712.1:p.Pro332=