Canonical Allele Identifier: CA1362082520

Linked Data

dbSNP Id: rs1701693055

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373257_46373258insGCCTTTTGCAGT , CM000665.2:g.46373257_46373258insGCCTTTTGCAGT GRCh38
NC_000003.11:g.46414748_46414749insGCCTTTTGCAGT , CM000665.1:g.46414748_46414749insGCCTTTTGCAGT GRCh37
NC_000003.10:g.46389752_46389753insGCCTTTTGCAGT NCBI36
NG_012637.1:g.8116_8117insGCCTTTTGCAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.355_356insGCCTTTTGCAGT (CCR5) MANE Select ENSP00000292303.4:p.Ile119delinsSerLeuLeu...
ENST00000292303.4:c.355_356insGCCTTTTGCAGT (CCR5) ENSP00000292303.4:p.Ile119delinsSerLeuLeu...
ENST00000445772.1:c.355_356insGCCTTTTGCAGT (CCR5) ENSP00000404881.1:p.Ile119delinsSerLeuLeu...
NM_000579.3:c.355_356insGCCTTTTGCAGT (CCR5) NP_000570.1:p.Ile119delinsSerLeuLeuGlnPhe...
NM_001100168.1:c.355_356insGCCTTTTGCAGT (CCR5) NP_001093638.1:p.Ile119delinsSerLeuLeuGln...
NR_125406.1:n.392-1841_392-1840insACTGCAAAAGGC (CCR5AS)
NM_000579.4:c.355_356insGCCTTTTGCAGT (CCR5) NP_000570.1:p.Ile119delinsSerLeuLeuGlnPhe...
NM_001100168.2:c.355_356insGCCTTTTGCAGT (CCR5) NP_001093638.1:p.Ile119delinsSerLeuLeuGln...
NM_001394783.1:c.355_356insGCCTTTTGCAGT (CCR5) MANE Select NP_001381712.1:p.Ile119delinsSerLeuLeuGln...