Canonical Allele Identifier: CA1047500337

Linked Data

dbSNP Id: rs1701689540

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373150_46373173del , CM000665.2:g.46373150_46373173del GRCh38
NC_000003.11:g.46414641_46414664del , CM000665.1:g.46414641_46414664del GRCh37
NC_000003.10:g.46389645_46389668del NCBI36
NG_012637.1:g.8009_8032del

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.248_271del (CCR5) MANE Select ENSP00000292303.4:p.Val83_Ala90del
ENST00000292303.4:c.248_271del (CCR5) ENSP00000292303.4:p.Val83_Ala90del
ENST00000445772.1:c.248_271del (CCR5) ENSP00000404881.1:p.Val83_Ala90del
NM_000579.3:c.248_271del (CCR5) NP_000570.1:p.Val83_Ala90del
NM_001100168.1:c.248_271del (CCR5) NP_001093638.1:p.Val83_Ala90del
NR_125406.1:n.392-1753_392-1730del (CCR5AS)
NM_000579.4:c.248_271del (CCR5) NP_000570.1:p.Val83_Ala90del
NM_001100168.2:c.248_271del (CCR5) NP_001093638.1:p.Val83_Ala90del
NM_001394783.1:c.248_271del (CCR5) MANE Select NP_001381712.1:p.Val83_Ala90del