Canonical Allele Identifier: CA1362082332

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372899_46372900delinsCA , CM000665.2:g.46372899_46372900delinsCA GRCh38
NC_000003.11:g.46414390_46414391delinsCA , CM000665.1:g.46414390_46414391delinsCA GRCh37
NC_000003.10:g.46389394_46389395delinsCA NCBI36
NG_012637.1:g.7758_7759delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.-4_-3delinsCA (CCR5) MANE Select ENSP00000292303.4:n.-4_-3delinsCA
ENST00000292303.4:c.-4_-3delinsCA (CCR5) ENSP00000292303.4:n.-4_-3delinsCA
ENST00000445772.1:c.-4_-3delinsCA (CCR5) ENSP00000404881.1:n.-4_-3delinsCA
NM_000579.3:c.-4_-3delinsCA (CCR5) NP_000570.1:n.-4_-3delinsCA
NM_001100168.1:c.-4_-3delinsCA (CCR5) NP_001093638.1:n.-4_-3delinsCA
NR_125406.1:n.392-1483_392-1482delinsTG (CCR5AS)
NM_000579.4:c.-4_-3delinsCA (CCR5) NP_000570.1:n.-4_-3delinsCA
NM_001100168.2:c.-4_-3delinsCA (CCR5) NP_001093638.1:n.-4_-3delinsCA
NM_001394783.1:c.-4_-3delinsCA (CCR5) MANE Select NP_001381712.1:n.-4_-3delinsCA