Canonical Allele Identifier: CA2665436388

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373328_46373336del , CM000665.2:g.46373328_46373336del GRCh38
NC_000003.11:g.46414819_46414827del , CM000665.1:g.46414819_46414827del GRCh37
NC_000003.10:g.46389823_46389831del NCBI36
NG_012637.1:g.8187_8195del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.426_434del (CCR5) MANE Select ENSP00000292303.4:p.Thr143_Gly145del
ENST00000292303.4:c.426_434del (CCR5) ENSP00000292303.4:p.Thr143_Gly145del
ENST00000445772.1:c.426_434del (CCR5) ENSP00000404881.1:p.Thr143_Gly145del
NM_000579.3:c.426_434del (CCR5) NP_000570.1:p.Thr143_Gly145del
NM_001100168.1:c.426_434del (CCR5) NP_001093638.1:p.Thr143_Gly145del
NR_125406.1:n.392-1919_392-1911del (CCR5AS)
NM_000579.4:c.426_434del (CCR5) NP_000570.1:p.Thr143_Gly145del
NM_001100168.2:c.426_434del (CCR5) NP_001093638.1:p.Thr143_Gly145del
NM_001394783.1:c.426_434del (CCR5) MANE Select NP_001381712.1:p.Thr143_Gly145del