Canonical Allele Identifier: CA1362082451

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373133_46373134delinsGT , CM000665.2:g.46373133_46373134delinsGT GRCh38
NC_000003.11:g.46414624_46414625delinsGT , CM000665.1:g.46414624_46414625delinsGT GRCh37
NC_000003.10:g.46389628_46389629delinsGT NCBI36
NG_012637.1:g.7992_7993delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.231_232delinsGT (CCR5) MANE Select ENSP00000292303.4:p.Leu77=
ENST00000292303.4:c.231_232delinsGT (CCR5) ENSP00000292303.4:p.Leu77=
ENST00000445772.1:c.231_232delinsGT (CCR5) ENSP00000404881.1:p.Leu77=
NM_000579.3:c.231_232delinsGT (CCR5) NP_000570.1:p.Leu77=
NM_001100168.1:c.231_232delinsGT (CCR5) NP_001093638.1:p.Leu77=
NR_125406.1:n.392-1717_392-1716delinsAC (CCR5AS)
NM_000579.4:c.231_232delinsGT (CCR5) NP_000570.1:p.Leu77=
NM_001100168.2:c.231_232delinsGT (CCR5) NP_001093638.1:p.Leu77=
NM_001394783.1:c.231_232delinsGT (CCR5) MANE Select NP_001381712.1:p.Leu77=