Canonical Allele Identifier: CA2740411609

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373915_46373916insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA , CM000665.2:g.46373915_46373916insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA GRCh38
NC_000003.11:g.46415406_46415407insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA , CM000665.1:g.46415406_46415407insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA GRCh37
NC_000003.10:g.46390410_46390411insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA NCBI36
NG_012637.1:g.8774_8775insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) MANE Select ENSP00000292303.4:p.Tyr339LeufsTer39
ENST00000292303.4:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) ENSP00000292303.4:p.Tyr339LeufsTer39
ENST00000445772.1:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) ENSP00000404881.1:p.Tyr339LeufsTer?
NM_000579.3:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) NP_000570.1:p.Tyr339LeufsTer39
NM_001100168.1:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) NP_001093638.1:p.Tyr339LeufsTer39
NR_125406.1:n.392-2499_392-2498insTAGTGCATGTTCTTTGTGGGCTAACTCTAGCGTCAATAAAAATGTTAAG (CCR5AS)
NM_000579.4:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) NP_000570.1:p.Tyr339LeufsTer39
NM_001100168.2:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) NP_001093638.1:p.Tyr339LeufsTer39
NM_001394783.1:c.1013_1014insCTTAACATTTTTATTGACGCTAGAGTTAGCCCACAAAGAACATGCACTA (CCR5) MANE Select NP_001381712.1:p.Tyr339LeufsTer39