Canonical Allele Identifier: CA2577573857

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373325_46373327del , CM000665.2:g.46373325_46373327del GRCh38
NC_000003.11:g.46414816_46414818del , CM000665.1:g.46414816_46414818del GRCh37
NC_000003.10:g.46389820_46389822del NCBI36
NG_012637.1:g.8184_8186del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.423_425del (CCR5) MANE Select ENSP00000292303.4:p.Val142del
ENST00000292303.4:c.423_425del (CCR5) ENSP00000292303.4:p.Val142del
ENST00000445772.1:c.423_425del (CCR5) ENSP00000404881.1:p.Val142del
NM_000579.3:c.423_425del (CCR5) NP_000570.1:p.Val142del
NM_001100168.1:c.423_425del (CCR5) NP_001093638.1:p.Val142del
NR_125406.1:n.392-1910_392-1908del (CCR5AS)
NM_000579.4:c.423_425del (CCR5) NP_000570.1:p.Val142del
NM_001100168.2:c.423_425del (CCR5) NP_001093638.1:p.Val142del
NM_001394783.1:c.423_425del (CCR5) MANE Select NP_001381712.1:p.Val142del