Canonical Allele Identifier: CA1362082779

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373780_46373781delinsAC , CM000665.2:g.46373780_46373781delinsAC GRCh38
NC_000003.11:g.46415271_46415272delinsAC , CM000665.1:g.46415271_46415272delinsAC GRCh37
NC_000003.10:g.46390275_46390276delinsAC NCBI36
NG_012637.1:g.8639_8640delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.878_879delinsAC (CCR5) MANE Select ENSP00000292303.4:p.Asn293=
ENST00000292303.4:c.878_879delinsAC (CCR5) ENSP00000292303.4:p.Asn293=
ENST00000445772.1:c.878_879delinsAC (CCR5) ENSP00000404881.1:p.Asn293=
NM_000579.3:c.878_879delinsAC (CCR5) NP_000570.1:p.Asn293=
NM_001100168.1:c.878_879delinsAC (CCR5) NP_001093638.1:p.Asn293=
NR_125406.1:n.392-2364_392-2363delinsGT (CCR5AS)
NM_000579.4:c.878_879delinsAC (CCR5) NP_000570.1:p.Asn293=
NM_001100168.2:c.878_879delinsAC (CCR5) NP_001093638.1:p.Asn293=
NM_001394783.1:c.878_879delinsAC (CCR5) MANE Select NP_001381712.1:p.Asn293=