Canonical Allele Identifier: CA2665436444

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373452_46373513del , CM000665.2:g.46373452_46373513del GRCh38
NC_000003.11:g.46414943_46415004del , CM000665.1:g.46414943_46415004del GRCh37
NC_000003.10:g.46389947_46390008del NCBI36
NG_012637.1:g.8311_8372del

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.550_611del (CCR5) MANE Select ENSP00000292303.4:p.Tyr184ProfsTer23
ENST00000292303.4:c.550_611del (CCR5) ENSP00000292303.4:p.Tyr184ProfsTer23
ENST00000445772.1:c.550_611del (CCR5) ENSP00000404881.1:p.Tyr184ProfsTer23
NM_000579.3:c.550_611del (CCR5) NP_000570.1:p.Tyr184ProfsTer23
NM_001100168.1:c.550_611del (CCR5) NP_001093638.1:p.Tyr184ProfsTer23
NR_125406.1:n.392-2096_392-2035del (CCR5AS)
NM_000579.4:c.550_611del (CCR5) NP_000570.1:p.Tyr184ProfsTer23
NM_001100168.2:c.550_611del (CCR5) NP_001093638.1:p.Tyr184ProfsTer23
NM_001394783.1:c.550_611del (CCR5) MANE Select NP_001381712.1:p.Tyr184ProfsTer23