Canonical Allele Identifier: CA1362082635

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373497G= , CM000665.2:g.46373497G= GRCh38
NC_000003.11:g.46414988G= , CM000665.1:g.46414988G= GRCh37
NC_000003.10:g.46389992G= NCBI36
NG_012637.1:g.8356G=

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.595G= (CCR5) MANE Select ENSP00000292303.4:p.Val199=
ENST00000292303.4:c.595G= (CCR5) ENSP00000292303.4:p.Val199=
ENST00000445772.1:c.595G= (CCR5) ENSP00000404881.1:p.Val199=
NM_000579.3:c.595G= (CCR5) NP_000570.1:p.Val199=
NM_001100168.1:c.595G= (CCR5) NP_001093638.1:p.Val199=
NR_125406.1:n.392-2080C= (CCR5AS)
NM_000579.4:c.595G= (CCR5) NP_000570.1:p.Val199=
NM_001100168.2:c.595G= (CCR5) NP_001093638.1:p.Val199=
NM_001394783.1:c.595G= (CCR5) MANE Select NP_001381712.1:p.Val199=