Canonical Allele Identifier: CA2665436206

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373128_46373150del , CM000665.2:g.46373128_46373150del GRCh38
NC_000003.11:g.46414619_46414641del , CM000665.1:g.46414619_46414641del GRCh37
NC_000003.10:g.46389623_46389645del NCBI36
NG_012637.1:g.7987_8009del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.226_248del (CCR5) MANE Select ENSP00000292303.4:p.Asp76ProfsTer?
ENST00000292303.4:c.226_248del (CCR5) ENSP00000292303.4:p.Asp76ProfsTer?
ENST00000445772.1:c.226_248del (CCR5) ENSP00000404881.1:p.Asp76ProfsTer?
NM_000579.3:c.226_248del (CCR5) NP_000570.1:p.Asp76ProfsTer?
NM_001100168.1:c.226_248del (CCR5) NP_001093638.1:p.Asp76ProfsTer?
NR_125406.1:n.392-1732_392-1710del (CCR5AS)
NM_000579.4:c.226_248del (CCR5) NP_000570.1:p.Asp76ProfsTer?
NM_001100168.2:c.226_248del (CCR5) NP_001093638.1:p.Asp76ProfsTer?
NM_001394783.1:c.226_248del (CCR5) MANE Select NP_001381712.1:p.Asp76ProfsTer?