Canonical Allele Identifier: CA1362082356

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372945_46372946delinsTA , CM000665.2:g.46372945_46372946delinsTA GRCh38
NC_000003.11:g.46414436_46414437delinsTA , CM000665.1:g.46414436_46414437delinsTA GRCh37
NC_000003.10:g.46389440_46389441delinsTA NCBI36
NG_012637.1:g.7804_7805delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.43_44delinsTA (CCR5) MANE Select ENSP00000292303.4:p.Tyr15=
ENST00000292303.4:c.43_44delinsTA (CCR5) ENSP00000292303.4:p.Tyr15=
ENST00000445772.1:c.43_44delinsTA (CCR5) ENSP00000404881.1:p.Tyr15=
NM_000579.3:c.43_44delinsTA (CCR5) NP_000570.1:p.Tyr15=
NM_001100168.1:c.43_44delinsTA (CCR5) NP_001093638.1:p.Tyr15=
NR_125406.1:n.392-1529_392-1528delinsTA (CCR5AS)
NM_000579.4:c.43_44delinsTA (CCR5) NP_000570.1:p.Tyr15=
NM_001100168.2:c.43_44delinsTA (CCR5) NP_001093638.1:p.Tyr15=
NM_001394783.1:c.43_44delinsTA (CCR5) MANE Select NP_001381712.1:p.Tyr15=