Canonical Allele Identifier: CA73686026

Linked Data

dbSNP Id: rs34962689

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373890_46373891insC , CM000665.2:g.46373890_46373891insC GRCh38
NC_000003.11:g.46415381_46415382insC , CM000665.1:g.46415381_46415382insC GRCh37
NC_000003.10:g.46390385_46390386insC NCBI36
NG_012637.1:g.8749_8750insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.988_989insC (CCR5) MANE Select ENSP00000292303.4:p.Glu330AlafsTer?
ENST00000292303.4:c.988_989insC (CCR5) ENSP00000292303.4:p.Glu330AlafsTer?
ENST00000445772.1:c.988_989insC (CCR5) ENSP00000404881.1:p.Glu330AlafsTer?
NM_000579.3:c.988_989insC (CCR5) NP_000570.1:p.Glu330AlafsTer?
NM_001100168.1:c.988_989insC (CCR5) NP_001093638.1:p.Glu330AlafsTer?
NR_125406.1:n.392-2474_392-2473insG (CCR5AS)
NM_000579.4:c.988_989insC (CCR5) NP_000570.1:p.Glu330AlafsTer?
NM_001100168.2:c.988_989insC (CCR5) NP_001093638.1:p.Glu330AlafsTer?
NM_001394783.1:c.988_989insC (CCR5) MANE Select NP_001381712.1:p.Glu330AlafsTer?